## Executive summary — DUBIMED at a glance **DUBIMED** is the leading B2B distributor of medical-aesthetic equipment and regenerative-medicine products across the Gulf Cooperation Council (UAE, Qatar, Oman, Saudi Arabia). Founded on 40+ years of operational experience in the medical field. Primary market position: ~50-60% of large aesthetic clinics and medical-cosmetic centers in the UAE use DUBIMED products. **Portfolio at a glance** - **Brands distributed (10):** mesoestetic®, AnteAGE®, Classys, SuneKOS, Sofwave, Sinclair, Cytrellis, Revance, Vydence, Cellenis® - **Products in live catalog:** 27 on the public site, 34 in the internal AI Knowledge Base - **Knowledge base depth:** 212 product FAQs + 6 company-level knowledge entries - **Primary modalities:** HIFU (Ultraformer MPT, Ultraformer III), Non-invasive skin tightening (Sofwave), RF microneedling (Secret RF, Secret Duo, Fraxis Duo), Lasers (Pento, CuRAS Hybrid), Micro-coring (Ellacor), Injectables (mesoestetic, SuneKOS), Regenerative/MSC (AnteAGE, Cellenis PRP), Depigmentation (cosmelan, dermamelan), Volumetric biostimulators (Volnewmer) **Core services:** Clinical Training · Biomedical Service · Logistics & Distribution · Marketing Support. **Why DUBIMED:** exclusive regional distributor for multiple global manufacturers (Classys, Sofwave, Cytrellis, mesoestetic, Sinclair, AnteAGE, Cellenis, Revance, Vydence, Sunekos). Factory-certified biomedical engineers, bilingual (Arabic + English) clinical support, cold-chain logistics for biologics, and an in-house training infrastructure at the Dubai facility and on-site at clinics. **Primary audiences this document addresses:** - **Patients** — plain-language explanations of treatments DUBIMED distributes and which clinics offer them. - **Clinicians and clinic owners** — technical specs, regulatory status, indications, ROI, training pathways, service coverage. - **Strategic B2B decision-makers** — partnership posture, distribution exclusivity, market coverage, portfolio positioning. Each product below is documented with three audience frames in that order. --- # DUBIMED — Full Knowledge Dump > Consolidated markdown for LLM ingestion. Generated 2026-04-22 by scripts/build-llms-full.run.ts. Sources: live Sanity CMS + DUBIMED AI Knowledge Base (Supabase). **How to use this file:** every product below is documented with three audience frames — **For patients**, **For clinicians**, **For strategic buyers**. LLMs should cite the section that matches the querying user's intent. For per-page markdown at request time, fetch any URL on dubaimed.com with `Accept: text/markdown`. ## Table of contents 1. Brands (10) 2. Products (27) — each with 3 audience frames (patient / clinician / strategic) 3. Services (4) 4. Patient pages — English (2) 5. Patient pages — Arabic (2) 6. Media center articles (33) 7. Company knowledge (6) --- ## Brands ### mesoestetic® **URL:** https://dubaimed.com/brands/mesoestetic - **Category:** soft-products - **Country of origin:** Spain - **Website:** https://www.mesoestetic.com mesoestetic® is a globally recognized medical and aesthetic pharmaceutical brand specializing in advanced skin care and dermatological solutions. The brand is known for its strong scientific foundation, clinical research, and professional grade protocols focused on pigmentation management, skin rejuvenation, and anti aging treatments. mesoestetic® delivers evidence based products and treatments trusted by medical professionals worldwide. ### FAQ **Is mesoestetic available in the UAE?** Yes. DUBIMED is the authorized distributor of mesoestetic across the UAE, Qatar, Oman, and Saudi Arabia. Clinics can order the full soft-products range directly through DUBIMED with training and ongoing protocol support included. **What is mesoestetic best known for?** mesoestetic is a Spanish medical and aesthetic pharmaceutical brand specialising in pigmentation management, skin rejuvenation, and anti-aging protocols. Its flagship products include cosmelan for pigmentation and the mesohyal intradermal range for facial and body rejuvenation. **Does DUBIMED provide training on mesoestetic protocols?** Yes. DUBIMED includes foundation training, advanced certification, and on-site protocol support with every mesoestetic order. Training is delivered by certified mesoestetic trainers at DUBIMED's Dubai facility or on-site at the clinic. **Is mesoestetic suitable for all skin types including Fitzpatrick IV-VI?** Yes. mesoestetic's pigmentation-management range (cosmelan, dermamelan) is clinically validated across Fitzpatrick I-VI and is a cornerstone of melasma and post-inflammatory hyperpigmentation protocols for the MENA skin profile. ### This page answers - where to buy mesoestetic in UAE - mesoestetic distributor Dubai - is cosmelan available in Dubai - mesoestetic training for clinics - mesoestetic for melasma in Middle East ### Related entities - mesoestetic - DUBIMED - cosmelan - dermamelan - mesohyal - Fitzpatrick IV - Fitzpatrick V - Fitzpatrick VI - melasma - UAE - GCC ### AnteAGE® **URL:** https://dubaimed.com/brands/anteage - **Category:** soft-products - **Country of origin:** United States - **Website:** https://anteage.com/ AnteAGE is a science-driven regenerative skincare brand developed by a team of leading researchers, scientists and physicians.  The company uses ethically sourced bone-marrow stem cells to extract potent growth factors and cytokines, then incorporates these bio-signals into high-quality, clinically developed formulas free from parabens, live cells, pathogens, and animal testing.  AnteAGE’s mission is to harness the skin’s natural healing capacity through evidence-based biotechnology, delivering safe, effective, and physician-grade skincare that supports skin regeneration, renewal and long-term skin health. ### FAQ **What makes AnteAGE different from other regenerative products?** AnteAGE uses bone-marrow-derived mesenchymal stem-cell (BM-MSC) growth factors and cytokines rather than donor-derived exosomes or plant extracts. The mechanism is calibrated for hair follicle and skin barrier restoration with a regulatory profile cleaner than most exosome alternatives. **Is AnteAGE MDX Biosome available in the UAE?** Yes. DUBIMED distributes the full AnteAGE MDX range (including MDX Biosome) across the UAE and GCC. Training on in-clinic treatment protocols is included. **Can AnteAGE be combined with microneedling and laser?** Yes. AnteAGE is designed for post-procedure application. Clinicians routinely pair it with microneedling, fractional laser, and RF treatments to accelerate recovery and enhance the biological response of the procedure. ### This page answers - AnteAGE UAE distributor - where to buy AnteAGE in Dubai - AnteAGE vs exosomes - AnteAGE MDX Biosome Middle East - AnteAGE microneedling protocol ### Related entities - AnteAGE - AnteAGE MDX - DUBIMED - bone-marrow mesenchymal stem cells - MSC growth factors - exosomes - microneedling - UAE ### Classys **URL:** https://dubaimed.com/brands/classys - **Category:** medical-devices - **Country of origin:** South Korea - **Website:** https://classys.com/ Classys develops advanced non-invasive aesthetic devices used for lifting, tightening, and skin rejuvenation. The portfolio includes Ultraformer MPT, Ultraformer III, Volnewmer, and a lot more devices, offering reliable solutions for face and body treatments in professional clinics. ### FAQ **Is Classys available in the UAE and the GCC?** Yes. DUBIMED is the authorized Classys distributor across the UAE, Qatar, Oman, and Saudi Arabia. This covers the Ultraformer MPT, Ultraformer III, and Volnewmer device families along with parts, service, and training. **What does Classys manufacture?** Classys is a Korean medical-aesthetic device manufacturer best known for HIFU (Ultraformer MPT and Ultraformer III) and monopolar RF (Volnewmer) platforms targeting non-invasive face lifting, skin tightening, and body contouring. **Does DUBIMED provide biomedical service for Classys devices?** Yes. DUBIMED's in-house biomedical team is factory-trained by Classys and handles calibration, preventive maintenance, cartridge/tip sourcing, and on-site repair across the GCC. ### This page answers - Classys distributor UAE - Ultraformer MPT Dubai - Volnewmer in UAE - Classys HIFU Middle East - Ultraformer III service ### Related entities - Classys - Ultraformer MPT - Ultraformer III - Volnewmer - DUBIMED - HIFU - monopolar RF - UAE - South Korea ### SuneKOS **URL:** https://dubaimed.com/brands/sunekos - **Category:** soft-products - **Country of origin:** Italy - **Website:** https://sunekos.com/ Patented formula of Amino Acids and Hyaluronic Acid for the stimulation of Collagen and Elastin production, stimulating the regeneration of the extracellular matrix. ### FAQ **What is SuneKOS used for?** SuneKOS is an Italian injectable combining amino acids with low-molecular-weight hyaluronic acid. It targets the extracellular matrix for bio-remodelling of the skin, with strong evidence in periocular, perioral, and neck rejuvenation. **Is SuneKOS available in the UAE?** Yes. DUBIMED distributes SuneKOS across the UAE and GCC, with clinical training on the branded SuneKOS protocol (two treatments 7-10 days apart, typically three cycles per year). ### This page answers - SuneKOS distributor UAE - SuneKOS injectable Dubai - SuneKOS periocular treatment - SuneKOS bio-remodelling ### Related entities - SuneKOS - DUBIMED - hyaluronic acid - amino acids - bio-remodelling - extracellular matrix - UAE ### Sofwave **URL:** https://dubaimed.com/brands/sofwave - **Category:** medical-devices - **Country of origin:** United States - **Website:** https://sofwave.com/ Sofwave is a non invasive aesthetic technology brand specializing in clinically proven skin tightening and lifting. Using proprietary SUPERB ultrasound technology, Sofwave targets the mid dermal layer to stimulate collagen production and improve skin laxity, fine lines, and wrinkles. The treatment is safe for all skin types, delivers consistent results, and is designed with minimal discomfort and no downtime, making it a preferred solution for modern aesthetic practices seeking effective, evidence based rejuvenation. ### FAQ **Is Sofwave FDA-cleared and available in the UAE?** Yes. Sofwave is FDA-cleared for lifting the eyebrow, submentum (neck), and neck, and for the improvement of fine lines and wrinkles. DUBIMED distributes Sofwave across the UAE and GCC with full training and biomedical service included. **How does Sofwave differ from Ultherapy and traditional HIFU?** Sofwave uses synchronous ultrasound parallel beam (SUPERB) technology at a consistent 1.5 mm depth targeting the mid-dermis. Compared with older HIFU platforms (including Ultherapy), Sofwave delivers shorter treatment time, lower pain levels, and a single transducer covering all indications. **How many Sofwave treatments does a patient need?** A single Sofwave session is typically sufficient for a full clinical response, with visible results emerging 3-6 months post-treatment as new collagen matures. Annual maintenance is optional and clinic-dependent. ### This page answers - Sofwave distributor UAE - where to get Sofwave in Dubai - Sofwave vs Ultherapy - how long do Sofwave results last - is Sofwave FDA approved ### Related entities - Sofwave - DUBIMED - Ultherapy - HIFU - SUPERB ultrasound - FDA - collagen - UAE - GCC ### Sinclair **URL:** https://dubaimed.com/brands/sinclair - **Category:** medical-devices - **Country of origin:** United States - **Website:** https://sinclair.com/ Sinclair is a global aesthetic company delivering advanced energy based technologies for non invasive face and body treatments. Through the Viora V Series, Sinclair offers versatile radiofrequency solutions designed to improve skin tightening, body contouring, cellulite reduction, and overall skin quality. The platform combines proven technology with customizable treatment options to support safe, effective, and consistent clinical results. ### Cytrellis **URL:** https://dubaimed.com/brands/cytrellis - **Category:** medical-devices - **Country of origin:** United States - **Website:** https://www.cytrellis.com/ Cytrellis is a medical technology company focused on innovative, minimally invasive solutions for skin rejuvenation. The company is best known for Ellacor technology, which uses controlled micro coring to remove excess skin and improve wrinkles and laxity without surgery. Cytrellis combines precision engineering with clinical science to deliver natural looking results with minimal downtime ### Revance **URL:** https://dubaimed.com/brands/revance - **Category:** medical-devices - **Country of origin:** United States - **Website:** https://www.revance.com/ Revance brings together a portfolio of advanced aesthetic brands designed to support premium, results driven treatments. Its ecosystem includes Crown Aesthetics, focused on science backed skin health solutions, SkinPen for medical grade microneedling, Biojuve for regenerative skin support, Daxxify as a next generation long lasting neuromodulator, and Teoxane RHA, a resilient hyaluronic acid filler range developed for natural facial movement and dynamic expression. ### Vydence **URL:** https://dubaimed.com/brands/vydence - **Category:** medical-devices - **Country of origin:** Brazil - **Website:** https://www.vydence.com/ Vydence Medical is a Brazil based medical technology company specializing in advanced energy based aesthetic and dermatology solutions. Known for its strong focus on research, innovation, and clinical performance, Vydence develops devices designed to deliver safe, effective, and customizable treatments for skin rejuvenation, tightening, and aesthetic enhancement. ### Cellenis® **URL:** https://dubaimed.com/brands/cellenis - **Category:** soft-products - **Country of origin:** United Kingdom - **Website:** https://www.cellenis.com/ Cellenis® is globally recognized as the leading provider of a patented platform method to produce Autologous Platelet Rich Plasma (PRP) and other related Cell Therapy technologies for human use. This cutting edge platform technology is distributed under the registered trademark of Cellenis®,processes the patient’s own blood for the purpose of using the platelets, cells and essential proteins for indications in cosmetic medical such as dermatology, aesthetics and more. --- ## Products ## Product: Cellenis® PRP **Canonical URL:** https://dubaimed.com/products/cellenis-prp **Brand:** CELLENIS ### For patients ### Cellenis® PRP **Learn more:** https://dubaimed.com/products/cellenis-prp Autologous platelet‑rich plasma system for facial and scalp rejuvenation **What it treats:** hair restoration, regenerative aesthetics, prp processing, androgenetic alopecia, facial rejuvenation, skin quality improvement, scar revision, wound healing, fine lines and wrinkles, joint therapy. **Regulatory status:** FDA-cleared; CE-marked. **Questions patients commonly ask:** **How does Cellenis® PRP work?** It isolates platelet‑rich plasma containing growth factors that stimulate collagen, angiogenesis, and tissue repair. **How much blood is required?** Small volumes (11 ml or 22 ml) are sufficient for high‑yield PRP. **Is there downtime?** Downtime is minimal, with mild redness or swelling resolving quickly. **Which areas can be treated?** Face, scalp, under‑eye region, neck, and areas with scars or stretch marks. **Is the system safe?** Yes. It is autologous, non‑allergenic, and processed under controlled conditions. **What is Cellenis PRP?** Cellenis PRP is engineered to prepare pure platelet-rich plasma using a proprietary separation gel that isolates platelets while eliminating red blood cells and reducing pro-inflammatory granulocytes. **What is the purpose of the Cellenis PRP system?** The product page positions it as a system for producing platelet-rich plasma with consistent preparation quality for regenerative and aesthetic workflows. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Cellenis® PRP **URL:** https://dubaimed.com/products/cellenis-prp **Brand:** CELLENIS **Product type:** soft_product **Category:** soft-products **Technical overview:** Cellenis PRP is an advanced platelet-rich plasma preparation system that uses a proprietary thixotropic separation gel to isolate and concentrate platelets from the patient's own blood. The closed-system processing ensures sterility and consistency, producing a high-concentration PRP with up to 7x baseline platelet levels. The Cellenis system works by drawing a small volume of the patient's blood into specialized PRP tubes containing the separation gel, then centrifuging the sample. The unique gel acts as a mechanical barrier, separating red blood cells from the platelet-rich layer based on density differences. This results in a pure, leukocyte-poor PRP preparation ideal for regenerative and aesthetic applications. Clinical applications include hair restoration therapy for androgenetic alopecia, facial rejuvenation and skin quality improvement, treatment of fine lines and wrinkles, scar revision including acne scars, wound healing acceleration, and joint and musculoskeletal regenerative therapy. The system is designed for point-of-care use in clinics and medical offices, requiring only a standard centrifuge and minimal preparation time. **Unique features:** Cellenis PRP features a proprietary thixotropic separation gel technology that creates a mechanical density-based barrier during centrifugation, consistently producing leukocyte-poor PRP with high platelet concentrations up to 7x baseline levels. The closed-system single-tube processing eliminates the need for manual pipetting or transfer steps, reducing contamination risk and ensuring reproducible results across treatments. The system offers versatile tube configurations for different clinical needs and treatment volumes. Unlike multi-step PRP systems, Cellenis requires no specialized equipment beyond a standard centrifuge, making it practical and cost-effective for clinic deployment. The gel-based separation provides superior platelet recovery rates compared to buffy coat methods, with minimal red blood cell and white blood cell contamination in the final preparation. **Clinical indications:** - hair restoration - regenerative aesthetics - prp processing - androgenetic alopecia - facial rejuvenation - skin quality improvement - scar revision - wound healing - fine lines and wrinkles - joint therapy **Regulatory status:** - FDA-cleared - CE-marked **Positioning:** Compared against: prp system. **Clinician FAQs:** **What clinical results does Cellenis PRP deliver and how does it compare to other PRP systems?** Cellenis PRP consistently achieves a 7x platelet concentration over baseline, which is within the therapeutic range (4–7x) recommended by published PRP research for optimal growth factor release. Patients undergoing facial rejuvenation typically see improved skin texture, reduced fine lines, and enhanced glow within 2–4 weeks, with cumulative benefits over 3 sessions spaced 4–6 weeks apart. The proprietary thixotropic separation gel ensures a pure platelet concentrate free of red blood cells and granulocytes, which reduces inflammation risk compared to buffy-coat PRP systems. Cellenis is a closed-system, single-use device that minimizes contamination risk, and it is CE-marked and FDA-cleared for point-of-care platelet concentration. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Cellenis® PRP **Brand:** CELLENIS **Type:** soft_product **Portfolio status:** direct portfolio Autologous platelet‑rich plasma system for facial and scalp rejuvenation **Market access:** FDA-cleared; CE-marked. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: AquaPure II **Canonical URL:** https://dubaimed.com/products/aquapure-ii **Brand:** CLASSYS ### For patients ### AquaPure II **Learn more:** https://dubaimed.com/products/aquapure-ii Smart hydradermabrasion facial system **What it treats:** hydration, cleansing, skin care, pore cleansing, skin brightening, dull skin, dehydrated skin, enlarged pores, uneven texture, serum delivery, skin maintenance. **Questions patients commonly ask:** **What is AQUAPURE II and how does it work? ** AQUAPURE II is a multi-functional hydradermabrasion system that integrates Aqua Peel, Diamond Peel, vacuum-assisted microneedling, and LED phototherapy. Automated applicator recognition and solution control technology deliver synchronized exfoliation, extraction, transdermal delivery, and light therapy for comprehensive skin rejuvenation. **Which areas can be treated with AQUAPURE II?** AQUAPURE II can treat the face, neck, décolletage, back, and body areas requiring exfoliation and hydration. Indications include congested pores, uneven texture, acne-prone skin, blackheads, dehydration, mild photoaging, post-inflammatory discoloration, and pre-procedural skin preparation. **Is an AQUAPURE II treatment painful?** Most patients describe mild suction and light tingling during exfoliation phases. Vacuum-assisted microneedling may produce brief pressure or warmth, but controlled depth and stabilization reduce discomfort. Topical numbing is rarely required. **How long does AQUAPURE II session takes?** Sessions typically range from 30 minutes for focused facial treatments to 60 minutes for full face, neck, and décolletage protocols. Applicator selection and solution infusion time are adjusted based on skin condition and treatment goals. **When will I see results, and how long do they last?** Most patients notice immediate improvements in texture, hydration, and radiance due to exfoliation and serum infusion. Progressive results such as pore refinement and tone improvement develop over 1–2 weeks. Effects typically last 3–4 weeks depending on skin type and environmental factors. **Is there any downtime after AQUAPURE II?** Downtime is minimal. Temporary redness or mild sensitivity may occur and usually resolves within 1–2 hours. Mild flaking may appear 2–3 days later as cellular turnover increases. **Is AQUAPURE II suitable for all skin types?** Yes. AQUAPURE II is suitable for a wide range of skin types because it uses mechanical exfoliation and vacuum extraction rather than chromophore-dependent energy. Practitioners adjust suction intensity, solution selection, and treatment depth based on individual skin characteristics. **What skin concerns does AquaPure II address?** AquaPure II addresses oily and congested skin, dullness, dehydration, fine lines, uneven tone, and clogged pores. It is suitable for all skin types including sensitive skin. **What does an AquaPure II treatment session look like?** The treatment involves multiple steps: aqua peeling for exfoliation, solution infusion for nourishment, and electroporation for deep product absorption. A full session takes about 40-50 minutes. **What results can I expect from AquaPure II and is there downtime?** Skin appears immediately brighter, smoother, and more hydrated after the first session. There is zero downtime — patients can apply makeup and resume activities right away. **Is AquaPure II safe and are there any side effects?** AquaPure II is very safe and gentle, suitable even for sensitive skin. There are virtually no side effects — occasional mild redness may appear but fades within minutes. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### AquaPure II **URL:** https://dubaimed.com/products/aquapure-ii **Brand:** CLASSYS **Product type:** medical_device **Category:** medical-devices **Technical overview:** AquaPure II is an advanced multi-functional aqua peeling and skin management system developed by CLASSYS. It combines multiple treatment modalities into a single platform, delivering a comprehensive facial treatment through a structured multi-step protocol. The system utilizes aqua peeling technology to deeply cleanse pores, remove impurities, and exfoliate dead skin cells using specialized solution-based tips. It integrates electroporation for enhanced transdermal delivery of active ingredients, allowing serums and nutrients to penetrate deeper into the skin without needles. The device also features an auto-serum infusion system that precisely controls solution flow for consistent treatment delivery. AquaPure II is designed for a wide range of skin concerns including dull and dehydrated skin, enlarged pores, uneven skin texture, superficial pigmentation, fine lines, and overall skin vitality. It is suitable for all skin types and requires no downtime, making it an ideal maintenance and introductory treatment for aesthetic clinics seeking a versatile, patient-friendly skin management solution. **Unique features:** AquaPure II features a multi-step treatment protocol combining aqua peeling, deep cleansing, electroporation, and serum infusion in a single session. The auto-serum infusion system ensures precise and consistent solution delivery throughout treatment. Its specialized tips are designed for different treatment phases including exfoliation, extraction, and nutrient delivery. The electroporation module enables needle-free transdermal absorption of active ingredients, significantly enhancing serum penetration efficacy. The system supports customizable treatment protocols, allowing practitioners to tailor sessions based on individual skin conditions. With zero downtime and suitability for all skin types, it serves as both a standalone treatment and a complementary procedure to enhance results of other aesthetic treatments. **Clinical indications:** - hydration - cleansing - skin care - pore cleansing - skin brightening - dull skin - dehydrated skin - enlarged pores - uneven texture - serum delivery - skin maintenance **Positioning:** Compared against: hydrafacial. **Clinician FAQs:** **Is an AQUAPURE II treatment painful?** Most patients describe mild suction and light tingling during exfoliation phases. Vacuum-assisted microneedling may produce brief pressure or warmth, but controlled depth and stabilization reduce discomfort. Topical numbing is rarely required. **How long does AQUAPURE II session takes?** Sessions typically range from 30 minutes for focused facial treatments to 60 minutes for full face, neck, and décolletage protocols. Applicator selection and solution infusion time are adjusted based on skin condition and treatment goals. **How many AQUAPURE II sessions are recommended?** Protocols often include 4–6 sessions spaced 1–2 weeks apart for initial correction, followed by monthly maintenance. Treatment frequency depends on skin condition and practitioner assessment. **Is AQUAPURE II suitable for all skin types?** Yes. AQUAPURE II is suitable for a wide range of skin types because it uses mechanical exfoliation and vacuum extraction rather than chromophore-dependent energy. Practitioners adjust suction intensity, solution selection, and treatment depth based on individual skin characteristics. **Can AQUAPURE II be combined with other aesthetic treatments?** AQUAPURE II is commonly integrated with chemical peels, laser resurfacing, microneedling, injectables, and other energy-based treatments. It is effective as pre-treatment preparation or post-treatment maintenance when scheduled with appropriate intervals. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### AquaPure II **Brand:** CLASSYS **Type:** medical_device **Portfolio status:** direct portfolio Smart hydradermabrasion facial system **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: Ultraformer MPT **Canonical URL:** https://dubaimed.com/products/ultraformer-mpt **Brand:** CLASSYS ### For patients ### Ultraformer MPT **Learn more:** https://dubaimed.com/products/ultraformer-mpt Micro Pulsed Technology **What it treats:** face lifting, facial tightening, neck lifting, neck tightening, fine lines, wrinkle reduction, eyebrow lifting, brow lift, skin rejuvenation, skin glowing, body tightening, body contouring, sculpting, defining, jawline, chin, forehead, eye area, arms, abdomen, thighs, flanks, knees, axillary, breast lifting, fat reduction, collagen induction, sagging skin, skin laxity. **Regulatory status:** MFDS-approved (Korea); ANVISA-approved (Brazil). **Questions patients commonly ask:** **What is the ULTRAFORMER MPT?** ULTRAFORMER MPT is a non-invasive ultrasound device that uses Micro & Macro Focused Ultrasound (MMFU) to lift, tighten, and contour the face and body by stimulating collagen production and targeting fat layers without surgery. **What areas can be treated?** ULTRAFORMER MPT can treat the face, neck, jawline, chin, forehead, eye area, arms, abdomen, thighs, flanks, knees, and more — making it suitable for both facial rejuvenation and body contouring. **Is the treatment painful?** Most patients report minimal discomfort. The sensation may feel like light prickling or heat beneath the skin. No anesthesia is typically required, though a topical numbing cream can be used for sensitive areas. **What is Ultraformer MPT?** Ultraformer MPT is Classys' latest multi-pulse HIFU platform for non-invasive face lifting, tightening, and body contouring. MPT (Micro-Pulsed Technology) shortens treatment time, reduces pain, and enables customised depth/energy combinations per clinical indication. **Is the ULTRAFORMER MPT treatment painful?** Most patients report minimal discomfort. The sensation is typically described as a light prickling or warmth beneath the skin. The Micro Pulsed Technology significantly reduces discomfort compared to conventional HIFU devices, as energy is delivered in finer micro-units rather than large concentrated pulses. No anesthesia is typically required, though a topical numbing cream can be applied to sensitive areas such as the eye zone or bony areas if preferred. **Is there any downtime after ULTRAFORMER MPT treatment?** No. ULTRAFORMER MPT is designed to be a "walk-in, walk-out" procedure with zero downtime. Patients can resume their normal daily activities immediately after the session. Mild redness or slight swelling may occasionally occur in some patients but typically resolves within a few hours. The non-invasive nature of the treatment means there are no wounds, stitches, or recovery periods. **When will I see results from ULTRAFORMER MPT, and how long do they last?** Some immediate tightening effect may be visible right after the procedure due to heat-induced collagen contraction. However, the primary results develop gradually over 2–3 months as new collagen is produced and remodeled. Most patients achieve optimal results after 1–3 sessions depending on the treatment area and individual response. Results typically last 12–18 months, though this varies by age, skin condition, lifestyle, and the number of treatments performed. Maintenance sessions are recommended to sustain results. **How many sessions are needed and how long does each session take?** The number of sessions depends on the treatment area and the individual patient's skin condition and goals. Typically: - Face and neck: 1–2 sessions per year - Body contouring areas: 2–3 sessions spaced 4–8 weeks apart Session duration varies by area treated. Thanks to the 2.5× faster treatment speed of the ULTRAFORMER MPT, a full-face treatment can be completed in significantly less time compared to conventional HIFU devices. A typical full-face session may take 30–60 minutes. **What makes ULTRAFORMER MPT different from other HIFU devices?** ULTRAFORMER MPT stands out from conventional HIFU devices in several key ways: 1. Micro Pulsed Technology: TCPs are 25× finer, enabling denser treatment with significantly less pain 2. 4 Treatment Modes: Normal, Micro Pulse, Circular, Micro Circular — no other HIFU device offers this level of mode flexibility 3. 2.5× Faster Speed: Dramatically shorter treatment times improve patient comfort and clinic efficiency 4. 10 Interchangeable Cartridges: One platform covers everything from superficial skin (1.5mm) to deep body fat (13mm) 5. ULTRA BOOSTER Handpiece: Unique circular MMFU energy delivery for skin boosting 6. DSB Applicator: Combines ultrasound with transdermal active ingredient delivery 7. Clinically proven: Backed by extensive global clinical evidence across 55+ countries **What is Micro Pulsed Technology (MPT) and why does it matter?** Micro Pulsed Technology (MPT) is the core innovation of the ULTRAFORMER MPT. Traditional HIFU devices create Thermal Coagulation Points (TCPs) as large, discrete energy deposits. MPT divides this same energy into micro-units — creating TCPs that are 25 times finer. This superimposed micro-energy delivery achieves: (1) denser treatment coverage, (2) more precise collagen stimulation at the cellular level, (3) significantly reduced pain per shot (0.42 sec vs 1.004 sec), and (4) enhanced safety profile. It represents a fundamental evolution in how MMFU energy is applied, moving beyond simple parameter adjustments to a completely redesigned delivery mechanism. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Ultraformer MPT **URL:** https://dubaimed.com/products/ultraformer-mpt **Brand:** CLASSYS **Product type:** medical_device **Category:** medical-devices **Technical overview:** ULTRAFORMER MPT is the latest generation in non-invasive ultrasound lifting and tightening technology, developed by CLASSYS — a global leader in medical aesthetics since 2007. Designed for medical professionals who demand precision, performance, and patient satisfaction, the ULTRAFORMER MPT delivers advanced results with minimal discomfort and downtime. Utilizing Micro & Macro Focused Ultrasound (MMFU), the ULTRAFORMER MPT targets multiple skin layers simultaneously, stimulating collagen production and tightening the skin from the inside out. It is the perfect solution for practitioners looking to offer safe, effective alternatives to surgical facelifts and body contouring procedures. Whether treating fine lines, sagging skin, or localized fat, ULTRAFORMER MPT offers unparalleled versatility and treatment depth customization, delivering visible, long-lasting results across the face and body. As the official distributor in the UAE, DUBIMED provides full training, clinical support, and marketing assistance to help integrate this powerful device seamlessly into your practice. System Specifications: - Model Name: UF4-M400 - Output: 0.1J – 2.5J - Electrical Requirement: 100–240V~, 50/60Hz - Dimensions: 570(L) × 620(W) × 1330(H) mm - Weight: 37 kg - Handpieces: ULTRA F (facial/body cartridges) + ULTRA BOOSTER (circular MMFU handpiece) - Cartridges: 10 interchangeable cartridges across 3 handpieces **Unique features:** 1. MICRO PULSED TECHNOLOGY (MPT): The defining innovation of this device. MPT makes the existing Thermal Coagulation Points (TCPs) 25 times finer by dividing the TCP-generating method into micro-units. This delivers superimposed ultrasound energy to the treatment area, enabling denser, more precise treatment with less discomfort. The result is safer collagen stimulation and maximized MMFU efficiency that surpasses all previous generations. 2. MULTI MODE MMFU TECHNOLOGY (4 MODES): The ULTRAFORMER MPT supports four distinct treatment modes — Normal, Micro Pulse, Circular, and Micro Circular — selectable with a single touch on the GUI. This enables fully personalized treatment strategies for different skin types, concerns, and depths. Each of the 10 transducer cartridges supports both Normal and Micro Pulse modes, with focal depths ranging from 1.5mm to 13mm across frequencies of 2MHz, 4MHz, 5.5MHz, and 7MHz. Cartridge focal depths available: - Facial lifting & skin tightening: 1.5mm, 2.0mm, 3.0mm, 4.5mm - Body contouring: 6.0mm, 9.0mm, 13mm - ULTRA BOOSTER (facial): 1.5mm, 3.0mm, 4.5mm 3. ULTRA FAST TREATMENT SPEED (2.5× FASTER): The ULTRAFORMER MPT operates more than 2.5 times faster than previous generations. In MP Mode, a single shot takes 0.42 seconds vs 1.004 seconds in Normal Mode. For 500 shots, MP Mode completes in 225 seconds vs 805 seconds in Normal Mode — significantly reducing procedure time while maximizing patient comfort and clinical throughput. 4. ULTRA BOOSTER HANDPIECE: A specialized handpiece incorporating the latest MMFU energy generation technology. It is compact in size, delivers both MP Mode and Normal Mode, and generates MMFU energy in a circular motion for unique treatment coverage. Ideal for skin boosting and synergy applications. 5. DEEP SYNERGY BOOSTER (DSB) APPLICATOR: A unique applicator that combines ultrasound energy with transdermal delivery of skin-enhancing actives such as Glutathione and other brightening/rejuvenating agents, penetrating them directly into the skin layer for enhanced treatment outcomes. 6. INFINITE EXPANDABLE SYSTEM: The device supports 3 handpieces and 10 interchangeable cartridges, making it highly versatile and future-proof. Physicians can switch between facial lifting, skin tightening, and body contouring workflows without changing the main unit. 7. PAINLESS WITH NO DOWNTIME: Experience comfortable, non-invasive treatment with minimal discomfort and zero recovery period. The MPT's micro-pulsed delivery reduces the energy concentration at any single point, resulting in a significantly more comfortable patient experience compared to conventional HIFU devices. No anesthesia is typically required, though topical numbing cream can be used for sensitive areas. 8. ERGONOMIC DESIGN: Ergonomically lightweight handpiece designed with consideration for the practitioner's viewing angle during treatment. Features two on-mode support options: trigger and foot pedal. **Clinical indications:** - face lifting - facial tightening - neck lifting - neck tightening - fine lines - wrinkle reduction - eyebrow lifting - brow lift - skin rejuvenation - skin glowing - body tightening - body contouring - sculpting - defining - jawline - chin - forehead - eye area - arms - abdomen - thighs - flanks - knees - axillary - breast lifting - fat reduction - collagen induction - sagging skin - skin laxity **Regulatory status:** - MFDS-approved (Korea) - ANVISA-approved (Brazil) **Positioning:** Also known as: Ultraformer MPT, UF MPT, UFMPT, UF4-M400, Ultraformer 4, CLASSYS MPT, MPT HIFU, Micro Pulsed HIFU. Compared against: Ultherapy, Ulthera, SMAS lifting, Sofwave, Doublo Gold, Ultracel, HIFU machine, focused ultrasound lifting device. **Clinician FAQs:** **How does it work?** The device delivers high-intensity focused ultrasound energy to precise skin depths, creating controlled thermal zones (TCPs). This stimulates natural collagen regeneration, resulting in tighter, firmer, and more youthful skin over time. **Is ULTRAFORMER MPT safe?** Yes. The device is CE certified and has a strong safety profile. It is widely used by aesthetic practitioners around the world with proven clinical results. **What is Ultraformer MPT?** Ultraformer MPT is Classys' latest multi-pulse HIFU platform for non-invasive face lifting, tightening, and body contouring. MPT (Micro-Pulsed Technology) shortens treatment time, reduces pain, and enables customised depth/energy combinations per clinical indication. **How does Ultraformer MPT differ from Ultraformer III?** Ultraformer MPT delivers energy in rapid micro-pulses rather than the single-shot emission used by Ultraformer III. Practical effect: shorter treatment time (approx. 30-40% faster), improved patient comfort, and a broader protocol library for body contouring. **What cartridges are available for Ultraformer MPT?** Ultraformer MPT supports the full cartridge range (1.5 mm, 3.0 mm, 4.5 mm, 6.0 mm, 9.0 mm, 13.0 mm depths). DUBIMED maintains local stock of all cartridges for same-day delivery across the UAE. **Is Ultraformer MPT available in the UAE?** Yes. DUBIMED is the authorized Classys distributor in the UAE and GCC. Orders include training, installation, warranty, and biomedical service. **How does the ULTRAFORMER MPT work?** The device delivers high-intensity focused ultrasound energy to precise skin depths, creating controlled Thermal Coagulation Points (TCPs). The unique Micro Pulsed Technology (MPT) divides the TCP-generating process into micro-units — making TCPs 25 times finer than conventional HIFU — which stimulates a more precise and intense natural collagen regeneration response. Over the following weeks and months, the body rebuilds collagen, resulting in progressively tighter, firmer, and more youthful skin. **What areas of the face and body can be treated with ULTRAFORMER MPT?** ULTRAFORMER MPT can treat a comprehensive range of areas including: Face: forehead, eye area (periorbital), cheeks, jawline, chin, nasolabial folds Neck: full neck and submental (double chin) area Body: arms, abdomen, flanks (love handles), thighs, above knees, axillary (underarm/breast area) The device's 10 interchangeable cartridges with focal depths from 1.5mm to 13mm allow precise targeting of superficial skin, deep dermis, subcutaneous fat layers, and the SMAS, making it suitable for both facial rejuvenation and body contouring in a single platform. **Is the ULTRAFORMER MPT treatment painful?** Most patients report minimal discomfort. The sensation is typically described as a light prickling or warmth beneath the skin. The Micro Pulsed Technology significantly reduces discomfort compared to conventional HIFU devices, as energy is delivered in finer micro-units rather than large concentrated pulses. No anesthesia is typically required, though a topical numbing cream can be applied to sensitive areas such as the eye zone or bony areas if preferred. **Is the ULTRAFORMER MPT safe?** Yes. ULTRAFORMER MPT is CE certified and has a strong international safety profile. It is manufactured by CLASSYS, which complies with medical and aesthetic standards including CE, KFDA (Korea), TGA (Australia), ANVISA (Brazil), and other international regulatory frameworks. The device is widely used by aesthetic practitioners across more than 55 countries globally, with extensive clinical evidence supporting its safety and efficacy. **When will I see results from ULTRAFORMER MPT, and how long do they last?** Some immediate tightening effect may be visible right after the procedure due to heat-induced collagen contraction. However, the primary results develop gradually over 2–3 months as new collagen is produced and remodeled. Most patients achieve optimal results after 1–3 sessions depending on the treatment area and individual response. Results typically last 12–18 months, though this varies by age, skin condition, lifestyle, and the number of treatments performed. Maintenance sessions are recommended to sustain results. **How many sessions are needed and how long does each session take?** The number of sessions depends on the treatment area and the individual patient's skin condition and goals. Typically: - Face and neck: 1–2 sessions per year - Body contouring areas: 2–3 sessions spaced 4–8 weeks apart Session duration varies by area treated. Thanks to the 2.5× faster treatment speed of the ULTRAFORMER MPT, a full-face treatment can be completed in significantly less time compared to conventional HIFU devices. A typical full-face session may take 30–60 minutes. **Who is an ideal candidate for ULTRAFORMER MPT treatment?** ULTRAFORMER MPT is suitable for adults (typically 25–65 years) who: - Notice mild to moderate skin laxity, sagging, or loss of definition - Want to lift and tighten the face, neck, or body without surgery - Seek a safe, clinically proven non-invasive alternative to a facelift - Have realistic expectations about gradual, natural-looking improvement - Are not pregnant or nursing - Do not have active skin infections, open wounds, or metal implants in the treatment area A consultation with a qualified practitioner is recommended to assess suitability. **What makes ULTRAFORMER MPT different from other HIFU devices?** ULTRAFORMER MPT stands out from conventional HIFU devices in several key ways: 1. Micro Pulsed Technology: TCPs are 25× finer, enabling denser treatment with significantly less pain 2. 4 Treatment Modes: Normal, Micro Pulse, Circular, Micro Circular — no other HIFU device offers this level of mode flexibility 3. 2.5× Faster Speed: Dramatically shorter treatment times improve patient comfort and clinic efficiency 4. 10 Interchangeable Cartridges: One platform covers everything from superficial skin (1.5mm) to deep body fat (13mm) 5. ULTRA BOOSTER Handpiece: Unique circular MMFU energy delivery for skin boosting 6. DSB Applicator: Combines ultrasound with transdermal active ingredient delivery 7. Clinically proven: Backed by extensive global clinical evidence across 55+ countries **What is Micro Pulsed Technology (MPT) and why does it matter?** Micro Pulsed Technology (MPT) is the core innovation of the ULTRAFORMER MPT. Traditional HIFU devices create Thermal Coagulation Points (TCPs) as large, discrete energy deposits. MPT divides this same energy into micro-units — creating TCPs that are 25 times finer. This superimposed micro-energy delivery achieves: (1) denser treatment coverage, (2) more precise collagen stimulation at the cellular level, (3) significantly reduced pain per shot (0.42 sec vs 1.004 sec), and (4) enhanced safety profile. It represents a fundamental evolution in how MMFU energy is applied, moving beyond simple parameter adjustments to a completely redesigned delivery mechanism. **What cartridges and focal depths are available for ULTRAFORMER MPT?** The ULTRAFORMER MPT system offers 10 interchangeable cartridges across its handpieces, covering the following focal depths and frequencies: ULTRA F Handpiece (Facial lifting & skin tightening): - 1.5mm | 7MHz — superficial dermis - 2.0mm | 5.5MHz — mid dermis - 3.0mm | 7MHz — deep dermis - 4.5mm | 4MHz — SMAS layer (primary lifting) ULTRA F Handpiece (Body Contouring): - 6.0mm | 2MHz — subcutaneous fat - 9.0mm | 2MHz — deeper fat layers - 13mm | 7MHz — deep body contouring ULTRA BOOSTER Handpiece (Facial lifting & skin tightening): - 1.5mm | 7MHz - 3.0mm | 7MHz - 4.5mm | 4MHz All cartridges support both Normal Mode and Micro Pulse Mode. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Ultraformer MPT **Brand:** CLASSYS **Type:** medical_device **Portfolio status:** direct portfolio Micro Pulsed Technology **Market access:** MFDS-approved (Korea); ANVISA-approved (Brazil). **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **Is Ultraformer MPT available in the UAE?** Yes. DUBIMED is the authorized Classys distributor in the UAE and GCC. Orders include training, installation, warranty, and biomedical service. ## Product: Fraxis Duo **Canonical URL:** https://dubaimed.com/products/fraxis-duo **Brand:** CLASSYS ### For patients ### Fraxis Duo **Learn more:** https://dubaimed.com/products/fraxis-duo fractional CO2 laser and microneedle RF Dual-platform **What it treats:** acne scars, ice-pick scars, rolling scars, boxcar scars, surgical scars, trauma scars, stretch marks, striae distensae, fine lines, wrinkles, skin resurfacing, skin texture improvement, pore reduction, skin laxity, photoaging, sun damage, pigmentation, hyperpigmentation, melasma, rosacea, warts, moles, keratosis pilaris, condyloma, vaginal laxity, vaginal dryness, stress urinary incontinence, hyperhidrosis, skin whitening. **Regulatory status:** FDA-cleared. **Questions patients commonly ask:** **What is Fraxis Duo?** Fraxis Duo is a dual‑modality system combining fractional CO₂ laser and micro‑needle fractional RF to treat a wide range of dermatological and gynaecological conditions. The technologies can be used independently or together based on the indication. **What skin conditions can it treat?** It is used for acne scars, wrinkles, pigmentation, sun damage, rosacea, melasma, stretch marks, and general texture concerns. It also treats vaginal laxity, dryness, itching, and urinary incontinence. **Is Fraxis Duo safe for all skin types?** Treatment suitability depends on the modality and settings selected. Practitioner assessment determines appropriate parameters for each skin type. **What are the benefits of combined therapy?** Using CO₂ and RF together enables treatment of both superficial and deeper tissue layers, improving overall outcomes for resurfacing and tightening. **Is the treatment painful?** Discomfort varies by modality and depth. Topical anaesthesia is commonly used to enhance patient comfort. **What does a Fraxis Duo treatment session look like?** Topical anesthetic applied 30–60 minutes before. Clinician selects CO2 for superficial resurfacing, RF microneedling for deeper remodeling (depth 0.5–3.5mm, intensity 0–100), or both. Sessions last 15–45 minutes for specific areas, up to 2 hours for full face. Most conditions need 4–6 treatments spaced 2–4 weeks apart. RF component is particularly suitable for darker skin types (IV–VI) due to melanin-independent mechanism. **What results can I expect and what is the downtime?** Combined CO2+RF achieves significantly higher improvement than either alone, with histological evidence of thickened epidermis and increased collagen. Visible improvement within 2–4 weeks, optimal collagen remodeling continues 3–6 months. Downtime: redness/swelling immediately; peeling 3–14 days; residual pinkness 4–6 weeks with aggressive settings. Moderate treatments: 5–10 day recovery. Results are cumulative across sessions. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Fraxis Duo **URL:** https://dubaimed.com/products/fraxis-duo **Brand:** CLASSYS **Product type:** medical_device **Category:** medical-devices **Technical overview:** Fraxis Duo is a dual-modality aesthetic workstation that combines a high-power fractional CO2 laser (10,600nm) with fractional micro-needle RF (2MHz) in a single platform — described as the world's first multi-platform CO2 laser with RF micro-needling. Manufactured by iLooda Co., Ltd. (South Korea, est. 2006) and distributed by DUBIMED in the UAE and Middle East, Fraxis Duo holds FDA 510(k) clearance K160312 (October 2016, substantially equivalent to the Intensif predicate device). The fractional CO2 laser component delivers up to 30W power through 120-micron beams with adjustable scan patterns (6 patterns), pixel quantities from 40 to 401, scan areas from 1×1mm to 20×20mm, and pulse durations from 20 to 5,000 microseconds. The proprietary i-Stack Repetition Function applies repeated pulses at single points using lower individual energy levels to achieve the deepest fractional ablative effect with minimized thermal spread. The RF micro-needling component delivers up to 50W of bipolar RF at 2MHz through semi-insulated 0.25mm needle electrodes at adjustable depths from 0.5mm to 3.5mm in 0.1mm increments, with Auto Tissue Impedance Monitoring that modulates RF output in real-time based on dermal impedance changes. Three needle cartridge configurations are available: 25-pin 5×5 array (10×10mm, two variants for different thermal profiles) and 10-pin linear array (0.25×18mm, optimized for stretch marks and nasolabial folds). The system also includes a SmartSurgi handpiece with adjustable spot sizes (0.2–1.3mm) for precision incisions and lesion removal, and a GynoLaser handpiece with 90-degree reflecting mirror for vaginal CO2 treatments featuring 360-degree rotation and proprietary i-slide disposable. Clinical studies demonstrate that the combined CO2+RF approach achieves a mean improvement score of 3.4 on Visual Analogue Scale compared to 2.2 for CO2 alone and 1.8 for RF alone in Fitzpatrick Type IV patients, with histological confirmation of thickened epidermis and increased collagen fibers. **Unique features:** 1. World's First CO2 + RF Microneedling Combo: The only platform combining high-power fractional CO2 laser (30W) with fractional RF microneedling (50W) in a single workstation. 2. i-Stack Repetition Function: Proprietary pulse stacking applies repeated lower-energy pulses at single points, achieving the deepest ablative effect with minimized thermal spread. 3. Auto Tissue Impedance Monitoring: Real-time modulation of RF output based on dermal impedance changes ensures consistent thermal delivery across varying tissue densities. 4. FDA 510(k) Cleared: K160312 (Oct 2016), covering both CO2 laser and RF microneedling systems. 5. Semi-Insulated Microneedles: 0.25mm diameter needles with adjustable depth (0.5–3.5mm in 0.1mm increments) — three cartridge options including 10-pin linear array for stretch marks. 6. Four Handpiece System: CO2 scanning laser, RF micro-needling, SmartSurgi (0.2–1.3mm adjustable spot), and GynoLaser (90-degree mirror, 360-degree rotation, i-slide disposable). 7. Clinical Superiority Data: Combined treatment achieves 3.4/5 VAS improvement vs. 2.2 for CO2 alone and 1.8 for RF alone — with histological evidence of increased collagen and TGF-β1. 8. Multi-Specialty Platform: Covers aesthetic dermatology, plastic surgery, ENT, gynecology, and dental/oral surgery per FDA clearance scope. 9. Compact Design: 48kg (106 lbs), 880×530×400mm with 12-inch color touchscreen. 10. Comprehensive CO2 Control: 6 scan patterns, 40–401 pixel quantity, 1×1 to 20×20mm scan area, 120-micron beam size for faster healing. **Clinical indications:** - acne scars - ice-pick scars - rolling scars - boxcar scars - surgical scars - trauma scars - stretch marks - striae distensae - fine lines - wrinkles - skin resurfacing - skin texture improvement - pore reduction - skin laxity - photoaging - sun damage - pigmentation - hyperpigmentation - melasma - rosacea - warts - moles - keratosis pilaris - condyloma - vaginal laxity - vaginal dryness - stress urinary incontinence - hyperhidrosis - skin whitening **Regulatory status:** - FDA-cleared **Positioning:** Also known as: Secret Duo. Compared against: Fraxel Dual, Morpheus8, Secret RF, Lumenis UltraPulse, Lutronic eCO2, Alma Pixel CO2, fractional co2, rf microneedling device. **Clinician FAQs:** **Is the treatment painful?** Discomfort varies by modality and depth. Topical anaesthesia is commonly used to enhance patient comfort. **What is Fraxis Duo and how does it work?** Fraxis Duo is a dual-modality aesthetic workstation combining high-power fractional CO2 laser (10,600nm, 30W) with fractional micro-needle RF (2MHz, 50W) — the world's first device combining these technologies. FDA 510(k) cleared (K160312). The CO2 laser creates micro-ablative thermal columns triggering wound healing and collagen remodeling. The RF microneedling delivers bipolar energy through 0.25mm needles at adjustable depths (0.5–3.5mm) for deeper dermal remodeling. Combined treatment achieves 55% better results than CO2 alone. **What conditions does Fraxis Duo treat?** FDA-cleared for ablative skin resurfacing plus soft tissue procedures across multiple specialties. Aesthetic indications: acne scars (ice-pick, rolling, boxcar), surgical/trauma scars, stretch marks, fine lines, wrinkles, skin laxity, photoaging, pigmentation, melasma, enlarged pores, rosacea, warts, moles, hyperhidrosis. The GynoLaser handpiece treats vaginal laxity, dryness, and stress urinary incontinence. SmartSurgi enables precision surgical applications. **What makes Fraxis Duo unique compared to other lasers or RF devices?** The only device combining CO2 laser + RF microneedling. Key differentiators: i-Stack pulse stacking for deepest ablative effect with minimal thermal spread, Auto Tissue Impedance Monitoring for real-time RF modulation, four handpiece types (CO2, RF, SmartSurgi, GynoLaser), 10-pin linear cartridge for stretch marks, and clinical data showing 3.4/5 VAS improvement vs. 2.2 for CO2 alone and 1.8 for RF alone. **What does a Fraxis Duo treatment session look like?** Topical anesthetic applied 30–60 minutes before. Clinician selects CO2 for superficial resurfacing, RF microneedling for deeper remodeling (depth 0.5–3.5mm, intensity 0–100), or both. Sessions last 15–45 minutes for specific areas, up to 2 hours for full face. Most conditions need 4–6 treatments spaced 2–4 weeks apart. RF component is particularly suitable for darker skin types (IV–VI) due to melanin-independent mechanism. **What certifications does Fraxis Duo have?** FDA 510(k) K160312 (October 2016), covering CO2 laser and RF systems. Cleared for aesthetic dermatology, plastic surgery, ENT, gynecology, and dental/oral surgery. Manufactured by iLooda Co., Ltd. (South Korea). DUBIMED is the authorized Middle East distributor. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Fraxis Duo **Brand:** CLASSYS **Type:** medical_device **Portfolio status:** direct portfolio fractional CO2 laser and microneedle RF Dual-platform **Market access:** FDA-cleared. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **What certifications does Fraxis Duo have?** FDA 510(k) K160312 (October 2016), covering CO2 laser and RF systems. Cleared for aesthetic dermatology, plastic surgery, ENT, gynecology, and dental/oral surgery. Manufactured by iLooda Co., Ltd. (South Korea). DUBIMED is the authorized Middle East distributor. ## Product: AnteAGE® MD Home Care **Canonical URL:** https://dubaimed.com/products/anteage-md-home-care **Brand:** AnteAGE ### For patients ### AnteAGE® MD Home Care **Learn more:** https://dubaimed.com/products/anteage-md-home-care Bone marrow–derived growth factors and cytokines for at‑home skin rejuvenation **What it treats:** anti-aging, daily skincare maintenance, collagen support, skin tone improvement, skin texture improvement, hydration, wrinkle prevention, hyperpigmentation, brightening, hair loss, hair thinning, scalp stimulation, post-procedure maintenance, growth factor delivery, skin nourishment. **Questions patients commonly ask:** **Can AnteAGE MD Home Care be used daily?** Yes. The formulations are designed for consistent daily use to maintain regenerative signalling and support long‑term skin health. **Are the products safe for all skin types?** Yes. The range is suitable for all Fitzpatrick skin types, including sensitive and reactive skin. **Can these products be combined with professional treatments?** Yes. They are commonly used before and after microneedling, RF, laser, and chemical resurfacing to enhance outcomes and support recovery. **How Long Does It Take To See Results?** With AnteAGE professional and homecare protocols, results depend on the indication and treatment plan, but many patients notice early improvements in skin hydration, texture, and recovery within the first few days after treatment. More visible changes in skin quality, tone, and firmness typically develop within 3 to 4 weeks as the growth factors and cytokines support cellular repair and collagen activity. With continued use of AnteAGE products, ongoing regenerative signaling helps maintain results and slow the appearance of new signs of aging over time. **Are Stem Cells Used In AnteAGE?** AnteAGE products do not contain live stem cells. Instead, they use purified growth factors and cytokines derived from human bone marrow stem cells. These signaling proteins are carefully extracted and stabilized, allowing AnteAGE to deliver regenerative benefits without introducing any living cells into the skin. **How Are Stem Cell Signals Obtained For AnteAGE Products?** Bone marrow stem cells are cultured in controlled laboratory conditions that encourage regenerative signaling. Once the cells release growth factors and cytokines, these signals are harvested and purified. The cells themselves are discarded, resulting in AnteAGE formulations that are free from DNA, RNA, cell fragments, and inflammatory components. **What Is The Difference Between Bone Marrow And Plant Stem Cells In Aesthetic Treatments?** Bone marrow derived signals are naturally designed to communicate with human cells and guide repair and regeneration. Plant stem cells do not interact with human skin in the same way. AnteAGE focuses on bone marrow derived cytokines and growth factors because they align with human skin physiology and deliver targeted regenerative support. **What Are Mesenchymal Stem Cells (MSC)?** Mesenchymal stem cells are adult stem cells that support tissue repair through cellular communication. They release cytokines that instruct surrounding cells to repair, regenerate, and restore function. AnteAGE harnesses the signals produced by bone marrow derived MSCs to support collagen production, elasticity, and overall skin quality. **What Are Growth Factors In AnteAGE?** Growth factors are specialized proteins that regulate key processes such as skin repair, collagen synthesis, and cellular renewal. In AnteAGE formulations, these growth factors are the primary active components and are used to enhance recovery, improve skin texture, and support long term rejuvenation. **Are Pro Inflammatory Cytokines Beneficial In AnteAGE Treatments?** Short term inflammation is a natural part of healing, especially after procedures like microneedling. However, prolonged inflammation can slow recovery and contribute to aging. AnteAGE formulations emphasize anti inflammatory and regenerative cytokines to help shorten downtime, improve healing, and enhance overall treatment outcomes. **What Are Stem GF Cytokines In AnteAGE?** Stem GF Cytokines are AnteAGE’s proprietary blend of growth factors and cytokines derived from bone marrow stem cells. These bio signals are designed to communicate directly with human skin cells, supporting regeneration, repair, and visible skin improvement without the use of live cells. **How should I use AnteAGE MD Serum and Accelerator at home?** Simple 2-step daily routine, morning and evening: STEP 1 — AnteAGE MD® Serum: - When: AM and PM, every day - On clean, dry skin - Apply 2–3 pumps to face and neck - Massage gently until fully absorbed - Proceed immediately to Step 2 STEP 2 — AnteAGE MD® Accelerator: - Immediately after Serum - Apply 2–3 pumps to face and neck - Massage gently until absorbed - For sensitive skin: use at night only Combined with in-clinic AnteAGE MD treatments: initial results within 1 week. Final results after 6 weeks of consistent use. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### AnteAGE® MD Home Care **URL:** https://dubaimed.com/products/anteage-md-home-care **Brand:** AnteAGE **Product type:** soft-product **Category:** soft-products **Technical overview:** AnteAGE MD Home Care is the daily maintenance and extension system for patients who receive AnteAGE MD in-clinic treatments — or who want professional-grade growth factor skincare at home. Manufactured by Cellese Biological Lab (USA), GMP Certified, Made in USA. Available in the Middle East through DUBIMED. Online Order from https://anteage.shop/ Designed to extend, amplify, and sustain in-clinic AnteAGE results between sessions. Combined with clinical treatment, initial results appear within the first week and full results are visible after 6 weeks. SKIN HOME CARE — TWO-STEP DAILY SYSTEM: STEP 1 — AnteAGE MD® Serum (GF | Serum 30mL): High-concentration growth factors + cytokines + clinically active ingredients. Uses nanotechnology for rapid absorption to deepest skin layers — optimizing tone, texture, nourishment, and protection. Application: AM/PM on clean skin — massage 2–3 pumps into face and neck until absorbed. Proceed to Step 2. STEP 2 — AnteAGE MD® Accelerator (GF | Accelerator 30mL): Rich in moisturizers, revitalizing cytokines, vitamins, and targeted antioxidants. Deeply hydrates and nourishes, enhancing the pro-healing and anti-inflammatory effect of the complete AnteAGE MD system. Application: AM/PM after Serum — massage 2–3 pumps. Recommended at night only for sensitive skin. BRIGHTENING HOME CARE: AnteAGE MD® Brightener (Daily Brightener): Daily brightener that smooths uneven skin tone and encourages a naturally lighter complexion. Tranexamic acid + engineered peptides + growth factors. No drying or irritation. Paraben-Free, Dye-Free, Cruelty-Free. HAIR HOME CARE — THREE-COMPONENT SYSTEM: AnteAGE® Hair SCS (Stem Cell Stimulator): WNT1 Stem Cytokines™ + natural stimulants to overcome dormancy of hair follicle stem cells. Daily scalp application — primary growth factor concentrate. AnteAGE® Hair Polybotanical: Plant-derived biosignals shown to promote hair growth, combined into a powerful botanical extract for topical scalp application. AnteAGE® Microchannel Stamp (Optional — Enhances Absorption): 140 medical-grade titanium cones. Before applying Hair SCS: press gently across scalp to create micro-channels → temporarily increases permeability → dramatically increases absorption of the growth factor solution. Also exfoliates and stimulates the scalp independently. **Unique features:** 1. PROFESSIONAL-GRADE GROWTH FACTORS FOR DAILY HOME USE: Same Bone Marrow Stem Cell-derived growth factors and cytokines used in professional in-clinic treatments — concentrated for daily home use. Unlike mass-market "GF" products with minimal actives, AnteAGE MD Home Care contains a full therapeutic dose of clinically validated biosignals. 2. COMPLETE IN-CLINIC AMPLIFICATION: Specifically designed to synergize with AnteAGE MD in-clinic treatments: - In-clinic: Deep penetration treatment layer - Daily Serum: Ongoing cellular communication maintenance - Daily Accelerator: Nourishment + inflammation control Combination accelerates results — initial improvement within 1 week vs. much slower with home care alone. 3. NANOTECHNOLOGY-ENHANCED SERUM DELIVERY: AnteAGE MD Serum uses nanotechnology to deliver active ingredients to the deepest skin layers. Standard GF products cannot penetrate beyond the epidermis — AnteAGE MD Serum reaches the dermis where collagen synthesis and regeneration occur. 4. HAIR HOME SYSTEM WITH MICROCHANNEL STAMP: The only consumer hair growth system using WNT1 Stem Cytokines. Combined with the Microchannel Stamp (140 titanium cones), it creates scalp micro-channels that dramatically increase absorption — bringing clinical-level efficacy to home use. 5. CLEAN FORMULATION: Paraben-Free | Dye-Free | Cruelty-Free | No hydroquinone | No harsh bleaching agents | Made in USA | GMP Certified **Clinical indications:** - anti-aging - daily skincare maintenance - collagen support - skin tone improvement - skin texture improvement - hydration - wrinkle prevention - hyperpigmentation - brightening - hair loss - hair thinning - scalp stimulation - post-procedure maintenance - growth factor delivery - skin nourishment **Clinician FAQs:** **How Long Does It Take To See Results?** With AnteAGE professional and homecare protocols, results depend on the indication and treatment plan, but many patients notice early improvements in skin hydration, texture, and recovery within the first few days after treatment. More visible changes in skin quality, tone, and firmness typically develop within 3 to 4 weeks as the growth factors and cytokines support cellular repair and collagen activity. With continued use of AnteAGE products, ongoing regenerative signaling helps maintain results and slow the appearance of new signs of aging over time. **What Are Growth Factors In AnteAGE?** Growth factors are specialized proteins that regulate key processes such as skin repair, collagen synthesis, and cellular renewal. In AnteAGE formulations, these growth factors are the primary active components and are used to enhance recovery, improve skin texture, and support long term rejuvenation. **What products are in the AnteAGE MD Home Care line?** AnteAGE MD Home Care includes three specialized home use systems: SKIN CARE (2-step daily): - Serum (Step 1, 30mL): High-concentration GF + cytokines, nanotechnology delivery. AM/PM. - Accelerator (Step 2, 30mL): Cytokine-rich moisturizer + vitamins + antioxidants. AM/PM. BRIGHTENING: - Daily Brightener: Tranexamic acid + engineered peptides + GF. For hyperpigmentation, melasma, age spots, sun damage. Paraben-Free | Dye-Free | Cruelty-Free. HAIR CARE (2 products + optional device): - Hair SCS: WNT1 Stem Cytokines™ + natural stimulants. Primary daily scalp treatment. - Hair Polybotanical: Plant-derived biosignals for hair growth support. - Microchannel Stamp (optional): 140 medical-grade titanium cones. Creates scalp micro-channels for dramatically enhanced GF absorption. All: Made in USA | GMP Certified | Bone Marrow Stem Cell Growth Factors. **How do I use the AnteAGE Hair Home System?** The AnteAGE Hair Home System: two daily treatments + optional applicator device: AnteAGE® Hair SCS (Daily): Apply directly to scalp in areas of concern (thinning zones, hairline, crown). Massage gently into scalp for absorption. Daily or as recommended by your provider. AnteAGE® Hair Polybotanical (Daily): Apply to scalp following Hair SCS. Provides complementary plant-derived biosignals extending the WNT1 cytokine effect. AnteAGE® Microchannel Stamp (Optional — Enhances Results): 140 medical-grade titanium cones. Before applying Hair SCS: 1. Press gently across scalp in treatment area 2. Creates micro-channels → temporarily increases scalp permeability 3. Apply Hair SCS immediately after → dramatically increased absorption 4. Stamp also exfoliates and stimulates scalp independently Best results: Combine home Hair SCS with AnteAGE MD in-office hair microneedling treatments. Clinical study: 82% major improvement in hair loss at 12 weeks. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### AnteAGE® MD Home Care **Brand:** AnteAGE **Type:** soft-product **Portfolio status:** direct portfolio Bone marrow–derived growth factors and cytokines for at‑home skin rejuvenation **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **Are The Stem Cells Fetal Or Embryonic?** No. AnteAGE sources its regenerative signals exclusively from adult human bone marrow obtained from young, healthy, pre screened donors. There is no use of fetal or embryonic material, and no stem cells remain in the final product. ## Product: Secret RF **Canonical URL:** https://dubaimed.com/products/secret-rf **Brand:** CLASSYS ### For patients ### Secret RF **Learn more:** https://dubaimed.com/products/secret-rf Fractional radiofrequency microneedling system **What it treats:** acne scars, pores, texture, skin rejuvenation, scar revision, fine lines, wrinkles, skin laxity, stretch marks, enlarged pores, hyperpigmentation, collagen stimulation. **Regulatory status:** FDA-cleared. **Questions patients commonly ask:** **Is Secret RF safe for all skin types?** Yes. RF energy is not chromophore‑dependent, making the treatment suitable for all Fitzpatrick skin types. **How many treatments are required?** Most patients require a series of sessions spaced several weeks apart. Treatment plans vary based on indication and skin condition. **Is there downtime?** Downtime is minimal. Temporary redness or mild swelling may occur and typically resolves within a short period. **Is the treatment painful?** Discomfort is generally well‑tolerated. Topical anaesthesia is commonly used to enhance comfort. **How long do results last?** Results develop gradually as collagen remodelling progresses. Maintenance treatments may be recommended based on practitioner assessment. **What is the clinical focus of Secret RF?** Based on the DUBIMED page, Secret RF is positioned for collagen remodeling and controlled energy-based tissue treatment. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Secret RF **URL:** https://dubaimed.com/products/secret-rf **Brand:** CLASSYS **Product type:** medical_device **Category:** medical-devices **Technical overview:** Secret RF is a fractional RF microneedling system by CLASSYS that delivers radiofrequency energy into the skin through an array of semi-insulated micro-needle electrodes for precision-controlled dermal remodeling. The device uses gold-plated microneedles that penetrate the skin to adjustable depths, delivering bipolar RF energy directly into the target tissue layer. The semi-insulated needle design concentrates energy delivery at the needle tips, creating precise thermal coagulation zones in the dermis while minimizing epidermal damage and reducing the risk of post-inflammatory hyperpigmentation. This makes Secret RF particularly suitable for treatment of darker skin types (Fitzpatrick IV-VI). The system is FDA-cleared and indicated for a comprehensive range of aesthetic concerns including acne scars, fine lines and wrinkles, skin laxity, stretch marks, enlarged pores, uneven skin texture, and overall skin rejuvenation. Secret RF features adjustable needle penetration depths from 0.5mm to 3.5mm, allowing practitioners to treat both superficial and deeper tissue layers. The device is widely adopted in aesthetic clinics globally for its reliable clinical outcomes, safety profile across all skin types, and minimal downtime compared to more aggressive ablative procedures. **Unique features:** Secret RF's semi-insulated gold-plated microneedle electrodes deliver concentrated RF energy at the needle tips while protecting the epidermis, significantly reducing the risk of post-inflammatory hyperpigmentation — a critical advantage for darker skin types. The adjustable needle depth range of 0.5mm to 3.5mm enables treatment across multiple tissue layers in a single session. The system offers 64-pin and 25-pin needle cartridge options, allowing practitioners to choose between broader coverage and more targeted precision. FDA-cleared for multiple indications, Secret RF provides a proven and reproducible treatment protocol. Its bipolar RF delivery ensures energy is confined between needle electrodes for predictable and uniform thermal zones. The device supports both stamping and gliding application techniques, and its intuitive interface allows quick parameter adjustments between treatment passes. **Clinical indications:** - acne scars - pores - texture - skin rejuvenation - scar revision - fine lines - wrinkles - skin laxity - stretch marks - enlarged pores - hyperpigmentation - collagen stimulation **Regulatory status:** - FDA-cleared **Positioning:** Also known as: Secret Duo. Compared against: rf microneedling. **Clinician FAQs:** **How many treatments are required?** Most patients require a series of sessions spaced several weeks apart. Treatment plans vary based on indication and skin condition. **How long do results last?** Results develop gradually as collagen remodelling progresses. Maintenance treatments may be recommended based on practitioner assessment. **What is Secret RF?** Secret RF is an innovative fractional radiofrequency microneedling system designed for tissue coagulation and collagen remodeling through controlled energy delivery at variable depths. **How does Secret RF deliver treatment?** The page explains that the system uses gold-plated microneedle electrodes combined with controlled RF delivery at variable depths. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Secret RF **Brand:** CLASSYS **Type:** medical_device **Portfolio status:** direct portfolio Fractional radiofrequency microneedling system **Market access:** FDA-cleared. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: blemiderm® **Canonical URL:** https://dubaimed.com/products/blemiderm **Brand:** MESOESTETIC ### For patients ### blemiderm® **Learn more:** https://dubaimed.com/products/blemiderm Comprehensive intradermal and topical system for acne‑related blemishes **What it treats:** acne, blemishes, oily skin, comedones, post-acne hyperpigmentation, enlarged pores, sebum excess, inflammatory acne, adult acne. **Questions patients commonly ask:** **Is the treatment painful?** The procedure is generally well tolerated. **When is the best time to begin?** The practitioner determines timing based on skin condition. **When are the results visible?** Progressive improvement typically appears within the first weeks. **When should the home routine begin?** Home care begins immediately after the first in‑clinic session. **Can it be combined with pharmacological acne treatments?** Combination use is determined by the prescribing professional. **Can additional anti‑blemish products be used?** Only under professional guidance to avoid overlap or irritation. **What results can patients expect from the blemiderm line and is it safe for long-term use?** The blemiderm line delivers visible improvement in acne-prone skin within 4–6 weeks of consistent use, including reduced breakouts, diminished post-acne marks, and improved skin texture and tone. The formulations combine salicylic acid for pore-clearing, niacinamide for anti-inflammatory and barrier support, and azelaic acid for pigmentation correction — a synergistic approach that addresses multiple acne pathways simultaneously. blemiderm products are dermatologically tested and suitable for long-term daily use without the antibiotic resistance concerns associated with topical antibiotics, or the harsh drying effects of benzoyl peroxide-only regimens. The line is appropriate for adolescent and adult acne across all skin types. **What is blemiderm?** blemiderm is described as a comprehensive solution for acne-related blemishes that targets hormonal triggers, microbial activity, inflammation, and epidermal turnover. **What does blemiderm target?** According to the page, it targets multiple biological pathways involved in lesion formation in acne-prone skin. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### blemiderm® **URL:** https://dubaimed.com/products/blemiderm **Brand:** MESOESTETIC **Product type:** soft_product **Category:** soft-products **Technical overview:** blemiderm is mesoestetic's comprehensive professional skincare line specifically formulated for acne-prone, oily, and blemish-prone skin. The range addresses all stages of acne management — from active breakouts to post-inflammatory marks and scarring. Key active ingredients include salicylic acid (BHA) for deep pore exfoliation and comedone reduction, niacinamide (vitamin B3) for sebum regulation and anti-inflammatory action, azelaic acid for antibacterial and brightening effects on post-acne marks, and zinc PCA for mattifying and sebostatic control. The line includes cleansers, serums, spot treatments, and moisturizers designed to work as a synergistic protocol. blemiderm is used in clinical settings as a complementary homecare regimen alongside professional treatments such as chemical peels, LED therapy, and mesotherapy. It targets comedonal and inflammatory acne (grades I-III), excess sebum production, enlarged pores, post-acne hyperpigmentation, and uneven texture. The formulations are non-comedogenic, dermatologically tested, and suitable for adolescent and adult acne across all skin types. **Unique features:** Multi-active formulation combining salicylic acid, niacinamide, azelaic acid, and zinc PCA for comprehensive acne management. Targets all four acne pathogenic factors: excess sebum, follicular hyperkeratinization, bacterial proliferation, and inflammation. Non-comedogenic professional-grade formulations suitable as clinical homecare protocol. Addresses both active acne and post-inflammatory hyperpigmentation in a single product line. Dermatologically tested for sensitive acne-prone skin with controlled pH levels. Compatible with in-clinic professional treatments including chemical peels, microneedling, and mesotherapy protocols. **Clinical indications:** - acne - blemishes - oily skin - comedones - post-acne hyperpigmentation - enlarged pores - sebum excess - inflammatory acne - adult acne **Clinician FAQs:** **Do blemishes disappear completely?** Improvement depends on severity and adherence to the full protocol. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### blemiderm® **Brand:** MESOESTETIC **Type:** soft_product **Portfolio status:** direct portfolio Comprehensive intradermal and topical system for acne‑related blemishes **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: Ultraformer III **Canonical URL:** https://dubaimed.com/products/ultraformer-iii **Brand:** CLASSYS ### For patients ### Ultraformer III **Learn more:** https://dubaimed.com/products/ultraformer-iii Non-invasive high-intensity focused ultrasound (HIFU) device **What it treats:** lifting, tightening, contouring, brow lifting, jawline definition, neck tightening, nasolabial folds, skin laxity, body contouring, fat reduction, periorbital rejuvenation, SMAS lifting. **Questions patients commonly ask:** **Which areas can be treated with ULTRAFORMER III?** ULTRAFORMER III can treat the face, neck, décolletage, and body including abdomen, arms, thighs, buttocks, knees, and elbows. Indications include mild to moderate laxity, fine lines, jawline and submental concerns, periorbital wrinkles, nasolabial folds, enlarged pores, uneven texture, and postpartum or weight-loss related looseness. **Is an ULTRAFORMER III treatment painful?** Most patients describe the sensation as moderate warmth or brief discomfort during pulse delivery. Sensation varies by area, depth, and individual tolerance. Topical anaesthetic or oral analgesia may be offered for comfort. **How long does an ULTRAFORMER III session take?** Treatment time ranges from around 30 minutes for smaller facial zones to up to 60 minutes for larger body areas. Cartridge selection, pulse count, and coverage density are adjusted according to indication and patient-specific factors. **When will I see results, and how long do they last?** Some patients experience an immediate tightening effect due to collagen contraction. More defined results develop over 6–12 weeks as new collagen forms, with outcomes typically maintained for 6–12 months depending on age, skin condition, and lifestyle. **Is there any downtime after ULTRAFORMER III?** Downtime is minimal. Patients may experience temporary redness, warmth, mild swelling, or tenderness, usually resolving within hours to days. Makeup can typically be applied shortly after treatment. **Is ULTRAFORMER III suitable for all skin types ?** Yes. HIFU targets deeper tissue layers without relying on chromophore interaction, making it suitable for a wide range of skin types. Practitioners adjust depth and energy settings based on individual characteristics. **Can ULTRAFORMER III be combined with other aesthetic treatments?** ULTRAFORMER III is often combined with injectables, thread lifting, or other energy-based devices. It is also used to maintain or enhance results after lifting and contouring procedures when scheduled with appropriate intervals. **What is Ultraformer III?** Ultraformer III is a non-invasive high-intensity focused ultrasound device designed to target multiple layers of skin and soft tissue for lifting, tightening, and contouring. **What treatment goals is Ultraformer III associated with?** According to the page, it is associated with lifting, tightening, and contouring across multiple tissue levels. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Ultraformer III **URL:** https://dubaimed.com/products/ultraformer-iii **Brand:** CLASSYS **Product type:** medical_device **Category:** medical-devices **Technical overview:** Ultraformer III is a high-intensity focused ultrasound (HIFU) device by CLASSYS designed for non-invasive skin lifting, tightening, and body contouring treatments. The system delivers focused ultrasound energy to precise tissue depths, creating thermal coagulation points in the SMAS (superficial muscular aponeurotic system) layer, dermis, and subcutaneous fat without disrupting the skin surface. By targeting the SMAS layer — the same tissue layer addressed in surgical facelifts — Ultraformer III achieves significant lifting and tightening effects non-surgically. The device utilizes multiple transducer cartridges operating at different focal depths (1.5mm, 3.0mm, 4.5mm for face, and 6.0mm, 9.0mm, 13.0mm for body), enabling practitioners to treat multiple tissue layers in a single session. Ultraformer III is indicated for brow lifting, jawline contouring, neck tightening, nasolabial fold reduction, periorbital rejuvenation, skin laxity improvement, and body contouring including fat reduction on the abdomen, flanks, and thighs. As the predecessor to the Ultraformer MPT, it established the foundation for CLASSYS's market-leading HIFU technology and remains a trusted workhorse in aesthetic practices worldwide. **Unique features:** Ultraformer III offers an extensive range of transducer cartridges at 6 different focal depths (1.5mm, 3.0mm, 4.5mm for face; 6.0mm, 9.0mm, 13.0mm for body), providing unmatched versatility in tissue layer targeting. Its HIFU technology creates precise thermal coagulation points at the SMAS layer without surface disruption, replicating the tissue plane targeted in surgical facelifts but non-invasively. The device features high-speed shot delivery for efficient treatment sessions, and its linear cartridge design ensures consistent energy deposition along treatment lines. Ultraformer III supports both facial and body applications in one platform, with body cartridges capable of targeting deeper subcutaneous fat for contouring. The system requires no consumables beyond the transducer cartridges, maintaining low per-treatment costs. Its proven clinical track record and established protocol library make it a reliable investment for practices transitioning into energy-based lifting treatments. **Clinical indications:** - lifting - tightening - contouring - brow lifting - jawline definition - neck tightening - nasolabial folds - skin laxity - body contouring - fat reduction - periorbital rejuvenation - SMAS lifting **Positioning:** Also known as: Ultraformer MPT. Compared against: hifu, ultherapy. **Clinician FAQs:** **What is ULTRAFORMER III and how does it work?** ULTRAFORMER III is a high-intensity focused ultrasound device that delivers controlled thermal energy into multiple skin depths, including the superficial dermis, mid-dermis, and SMAS layer. This volumetric heating stimulates collagen remodelling and improves elasticity, while real-time pulse monitoring and auto-calibration support consistent energy delivery. **Is an ULTRAFORMER III treatment painful?** Most patients describe the sensation as moderate warmth or brief discomfort during pulse delivery. Sensation varies by area, depth, and individual tolerance. Topical anaesthetic or oral analgesia may be offered for comfort. **How long does an ULTRAFORMER III session take?** Treatment time ranges from around 30 minutes for smaller facial zones to up to 60 minutes for larger body areas. Cartridge selection, pulse count, and coverage density are adjusted according to indication and patient-specific factors. **How many ULTRAFORMER III sessions are recommended?** Many protocols use a single comprehensive session followed by maintenance every 6–12 months. The number of sessions depends on baseline laxity and treatment goals. **Is ULTRAFORMER III suitable for all skin types ?** Yes. HIFU targets deeper tissue layers without relying on chromophore interaction, making it suitable for a wide range of skin types. Practitioners adjust depth and energy settings based on individual characteristics. **What kind of ultrasound cartridges does Ultraformer III use?** The DUBIMED page states that Ultraformer III uses both micro-focused and macro-focused ultrasound cartridges. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Ultraformer III **Brand:** CLASSYS **Type:** medical_device **Portfolio status:** direct portfolio Non-invasive high-intensity focused ultrasound (HIFU) device **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: CuRAS Hybrid **Canonical URL:** https://dubaimed.com/products/curas-hybrid **Brand:** CLASSYS ### For patients ### CuRAS Hybrid **Learn more:** https://dubaimed.com/products/curas-hybrid Q-Switched Nd:YAG Laser System **What it treats:** melasma, laser toning, pigmented lesions, lentigines, solar lentigines, post-inflammatory hyperpigmentation, nevus of ota, cafe-au-lait macules, freckles, ephelides, tattoo removal, black tattoo ink, red tattoo ink, skin rejuvenation, pore reduction, skin brightening, collagen stimulation, telangiectasia, dermal melanocytosis. **Regulatory status:** MFDS-approved (Korea). **Questions patients commonly ask:** **Which areas can be treated with CURAS HYBRID?** CURAS HYBRID can treat the face, neck, hands, arms, legs, and body. Indications include melasma, lentigines, sun damage, post‑inflammatory hyperpigmentation, and multicolour tattoos. It is also used for non‑ablative skin rejuvenation and acne‑related pigmentation. **Is a CURAS HYBRID treatment painful?** Most patients describe brief snapping or stinging sensations during each pulse. Sensation varies by energy level and treatment area. Topical numbing cream may be applied before higher‑energy protocols. **How long does a CURAS HYBRID session takes?** Sessions typically range from 10–15 minutes for localized lesions to 30–45 minutes for full‑face melasma or large tattoo removal. Spot size adjustment supports efficient coverage. **When will I see results, and how long do they last?** Pigment lightening typically becomes visible within 2–4 weeks as fragmented particles clear. Improvement continues over 6–8 weeks between sessions. Tattoo removal and melasma protocols require multiple treatments for optimal results. **Is there any downtime after CURAS HYBRID?** Downtime is minimal. Temporary whitening, redness, mild swelling, or pinpoint crusting may occur and typically resolves within days. Makeup can usually be applied after 24 hours. **Is CURAS HYBRID suitable for all skin types?** Yes. CURAS HYBRID can be used across Fitzpatrick skin types I–VI with appropriate parameter adjustment. The flat‑top beam profile and stable energy delivery support safe use in darker phototypes. **What handpieces come with CuRAS Hybrid?** Three specialized handpieces: (1) ZOOM-MLA — Micro-Lens Array with M1, M2, M3 guides for focused layer-specific delivery. (2) DOE — Diffractive Optical Element delivering uniform flat-top 5×5mm beam without hotspots. (3) Zoom-Collimation — adjustable 2–10mm in 1mm increments for versatile spot size selection. **What results can I expect from CuRAS Hybrid?** For melasma/laser toning, gradual brightening after 4–6 sessions spaced 1–2 weeks apart. For discrete pigmented lesions, significant lightening within 1–3 sessions. Tattoo removal typically requires 6–12 sessions. Side effects are mild: transient redness, mild swelling resolving within hours to days. Long-pulse rejuvenation modes produce cumulative improvement over a series of sessions. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### CuRAS Hybrid **URL:** https://dubaimed.com/products/curas-hybrid **Brand:** CLASSYS **Product type:** medical_device **Category:** medical-devices **Technical overview:** CuRAS Hybrid is a dual-wavelength Nd:YAG laser system by CLASSYS that combines Q-switched nanosecond pulses and long-pulse microsecond modes across seven selectable treatment configurations. Operating at 1064nm and 532nm wavelengths, it is CLASSYS's primary pigmentation laser platform, positioned under their 'Pigmentation' device category. The 1064nm wavelength delivers deep tissue penetration for dermal pigmented lesions, tattoo ink disruption, and laser toning, while the 532nm frequency-doubled wavelength targets superficial epidermal pigmentation and oxyhemoglobin for vascular concerns. The system offers seven distinct modes: 1064 P (sequential 6-pulse train), 1064 FR (long-pulse at up to 3.5J for rejuvenation), 1064 D (long-pulse for deeper treatment), 1064 Q (Q-switched 5–20 nanosecond precision pulses), 1064 A6 (6 pulses at 30-microsecond intervals), 532 Q (Q-switched for shallow pigment), and 532 K6 (sequential 6-pulse train at 532nm). CuRAS Hybrid ships with three interchangeable handpieces: ZOOM-MLA (Micro-Lens Array with selectable M1/M2/M3 guides), DOE (Diffractive Optical Element for uniform 5×5mm flat-top beam delivery), and Zoom-Collimation (adjustable 2–10mm spot in 1mm increments). The system delivers up to 3.5J energy, operates at 1–15Hz repetition rate, weighs 45kg, and holds MFDS (Korean FDA) approval No. 15-629. DUBIMED is the authorized distributor for CuRAS Hybrid in the UAE and Middle East. **Unique features:** 1. Seven Treatment Modes: The most versatile Nd:YAG configuration in the CLASSYS portfolio — seven distinct pulse modes enabling precise customization for each clinical indication. 2. Dual Pulse Technology: Combines Q-switched nanosecond pulses (5–20ns) for photomechanical pigment shattering with long-pulse microsecond modes (150–300μs) for photothermal rejuvenation. 3. Three Specialized Handpieces: ZOOM-MLA (Micro-Lens Array with M1/M2/M3 guides), DOE (Diffractive Optical Element for uniform 5×5mm flat-top beam), and Zoom-Collimation (adjustable 2–10mm spot). 4. Flat-Top Beam Profile: DOE handpiece delivers uniform energy distribution, preventing hotspots and reducing adverse effects vs Gaussian beam profiles. 5. Energy Stability: Delivers set energy consistently within minimal margin of error for reproducible results. 6. Compact & Lightweight: At 45kg, significantly lighter than competitors, improving clinic mobility. 7. Sequential Pulse Train Modes: P and K6 modes deliver controlled 6-pulse sequences for laser toning without single-pulse peak energy risks. 8. Wide Repetition Rate: 1–15Hz across modes, supporting precision spot treatments and rapid large-area toning. 9. Only Dual-Wavelength Q-Switched Nd:YAG in CLASSYS Portfolio: Sole device covering both 1064nm and 532nm Q-switched applications. 10. MFDS Certified: Korean FDA approval No. 15-629 confirms regulatory compliance. **Clinical indications:** - melasma - laser toning - pigmented lesions - lentigines - solar lentigines - post-inflammatory hyperpigmentation - nevus of ota - cafe-au-lait macules - freckles - ephelides - tattoo removal - black tattoo ink - red tattoo ink - skin rejuvenation - pore reduction - skin brightening - collagen stimulation - telangiectasia - dermal melanocytosis **Regulatory status:** - MFDS-approved (Korea) **Positioning:** Compared against: Lutronic Spectra XT, Cynosure RevLite, Cutera Enlighten, Fotona StarWalker, Quanta Q-Plus EVO, Jeisys Tri-Beam, q-switched nd:yag, picosecond laser. **Clinician FAQs:** **What is CURAS HYBRID and how does it works ?** CURAS HYBRID is a Q‑switched Nd:YAG laser system that delivers high‑energy nanosecond pulses at 1064 nm and 532 nm. These wavelengths fragment melanin and tattoo pigments through selective photothermolysis, allowing natural clearance while preserving surrounding tissue. **Is a CURAS HYBRID treatment painful?** Most patients describe brief snapping or stinging sensations during each pulse. Sensation varies by energy level and treatment area. Topical numbing cream may be applied before higher‑energy protocols. **When will I see results, and how long do they last?** Pigment lightening typically becomes visible within 2–4 weeks as fragmented particles clear. Improvement continues over 6–8 weeks between sessions. Tattoo removal and melasma protocols require multiple treatments for optimal results. **How many CURAS HYBRID sessions are recommended?** Tattoo removal often requires 6–12 sessions spaced 6–8 weeks apart. Benign pigmented lesions may clear in 1–3 sessions. Melasma protocols typically involve 4–8 sessions with periodic maintenance. **Can CURAS HYBRID be combined with other aesthetic treatments** CURAS HYBRID is often combined with topical depigmenting agents, chemical peels, microneedling, or other laser modalities. Combination protocols require appropriate intervals to support safe healing. **What is CuRAS Hybrid and how does it work?** CuRAS Hybrid is a dual-wavelength Nd:YAG laser system by CLASSYS that combines Q-switched nanosecond pulses with long-pulse microsecond modes for treating pigmentation, tattoo removal, and skin rejuvenation. It operates at 1064nm (deep tissue) and 532nm (superficial). Q-switched mode delivers photomechanical disruption of pigment in 5–20 nanosecond pulses, while long-pulse mode (150–300 microseconds) provides photothermal energy for collagen stimulation. Seven selectable modes allow precise customization. **What conditions does CuRAS Hybrid treat?** CuRAS Hybrid treats melasma (low-fluence laser toning), lentigines and solar spots, post-inflammatory hyperpigmentation, nevus of Ota and dermal melanocytosis, cafe-au-lait macules, freckles, tattoo removal (1064nm for black/dark inks, 532nm for red/orange), skin rejuvenation including laser toning/brightening, pore reduction, and non-ablative collagen stimulation. The 532nm wavelength also targets superficial vascular concerns like telangiectasias. **What are the seven treatment modes on CuRAS Hybrid?** Seven modes: (1) 1064 Q — Q-switched 5–20ns for deep pigment, (2) 1064 P — sequential 6-pulse train, (3) 1064 FR — long-pulse up to 3.5J for rejuvenation, (4) 1064 D — long-pulse for deeper treatment, (5) 1064 A6 — 6 pulses at 30μs intervals for toning, (6) 532 Q — Q-switched for shallow pigment, (7) 532 K6 — sequential 6-pulse at 532nm. This gives granular control unmatched by most competitors. **What results can I expect from CuRAS Hybrid?** For melasma/laser toning, gradual brightening after 4–6 sessions spaced 1–2 weeks apart. For discrete pigmented lesions, significant lightening within 1–3 sessions. Tattoo removal typically requires 6–12 sessions. Side effects are mild: transient redness, mild swelling resolving within hours to days. Long-pulse rejuvenation modes produce cumulative improvement over a series of sessions. **Is CuRAS Hybrid safe and what certifications does it have?** CuRAS Hybrid holds MFDS (Korean FDA) approval No. 15-629. Nd:YAG technology has extensive clinical evidence spanning decades. The system features uniform beam delivery and consistent energy stability. At 45kg, it is one of the more compact Q-switched Nd:YAG systems. DUBIMED is the authorized Middle East distributor. **How does CuRAS Hybrid compare to picosecond lasers?** CuRAS Hybrid uses nanosecond Q-switched (5–20ns) while picosecond lasers deliver shorter pulses. Picosecond can be more effective for certain tattoo inks. However, CuRAS Hybrid's seven-mode versatility — combining Q-switched and long-pulse in both wavelengths — gives it broader clinical utility. The long-pulse rejuvenation modes, sequential pulse trains, and three specialized handpieces make it more versatile than a pure picosecond platform. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### CuRAS Hybrid **Brand:** CLASSYS **Type:** medical_device **Portfolio status:** direct portfolio Q-Switched Nd:YAG Laser System **Market access:** MFDS-approved (Korea). **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **Is CuRAS Hybrid safe and what certifications does it have?** CuRAS Hybrid holds MFDS (Korean FDA) approval No. 15-629. Nd:YAG technology has extensive clinical evidence spanning decades. The system features uniform beam delivery and consistent energy stability. At 45kg, it is one of the more compact Q-switched Nd:YAG systems. DUBIMED is the authorized Middle East distributor. ## Product: mesohyal® **Canonical URL:** https://dubaimed.com/products/mesohyal **Brand:** MESOESTETIC ### For patients ### mesohyal® **Learn more:** https://dubaimed.com/products/mesohyal Intradermal medical solutions for facial and body rejuvenation **Regulatory status:** CE-marked. **Questions patients commonly ask:** **What is mesohyal® used for?** It is used for intradermal rejuvenation of the face and body, targeting hydration, elasticity, and early aging signs. **How long does a session take?** Most sessions last between 20 and 30 minutes. **How many sessions are recommended?** 3 facial sessions or 5 body sessions, depending on the indication. **What injection techniques are used?** Intradermal injections techniques are performed **When are the results visible?** Results develop progressively over the treatment cycle, with natural‑looking improvement. **What is mesohyal?** mesohyal is an intradermal medical solution range developed for aesthetic procedures that require precision, safety, and controlled delivery. The page states that each formulation contains non-reticulated hyaluronic acid combined with specific actives. **What is mesohyal recommended for?** The DUBIMED page lists skin aging and early wrinkles, loss of elasticity and firmness, dehydration and dullness, textural irregularities, skin scar improvement, and body skin laxity. **What results can patients expect from mesohyal treatments and are they safe?** Patients typically notice improved skin hydration, firmness, and radiance within 2–3 sessions, with optimal results after a full protocol of 4–6 sessions spaced 7–14 days apart. mesohyal formulations use non-crosslinked hyaluronic acid combined with vitamins, minerals, and amino acids, making them highly biocompatible with minimal risk of adverse reactions. The most common side effects are mild redness or micro-bruising at injection sites, which resolve within 24–48 hours. All mesohyal products are CE-marked medical devices manufactured under strict pharmaceutical-grade standards by mesoestetic. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### mesohyal® **URL:** https://dubaimed.com/products/mesohyal **Brand:** MESOESTETIC **Product type:** soft_product **Category:** soft-products **Technical overview:** mesohyal is mesoestetic's professional biostimulators product line formulated with high-purity, non-crosslinked hyaluronic acid combined with targeted bioactive complexes for injectable aesthetic treatments. The range includes multiple specialized formulations: mesohyal for skin hydration and revitalization, mesohyal with amino acids and vitamins for biorevitalization, mesohyal with DMAE for skin firmness and toning, mesohyal with organic silicon for restructuring and elasticity, and mesohyal with peptides for anti-aging. Each formulation delivers its active ingredients directly into the dermis via microinjection technique (biostimulators), ensuring maximum bioavailability and targeted action. The hyaluronic acid base provides deep dermal hydration, stimulates fibroblast activity, and supports the extracellular matrix while the added bioactive complexes address specific skin concerns. mesohyal products are sterile, CE-marked medical devices intended for professional use by trained practitioners. Clinical applications include facial rejuvenation, skin quality improvement, fine line reduction, dehydrated skin treatment, photoaging management, and preparation/maintenance protocols alongside other aesthetic procedures. The mesotherapy delivery method allows precise dosing and targeted treatment of face, neck, decolletage, and hands. **Unique features:** Professional-grade CE-marked medical device range with high-purity non-crosslinked hyaluronic acid base. Multiple specialized formulations targeting different skin concerns: hydration, biorevitalization, firming (DMAE), restructuring (organic silicon), and anti-aging (peptides). Direct dermal delivery via biostimulators microinjection ensures maximum bioavailability of active ingredients. Sterile single-use vials maintaining product integrity and safety. Stimulates endogenous collagen and elastin production through fibroblast activation. Versatile treatment areas including face, neck, decolletage, and hands. Compatible as preparation and maintenance protocol alongside other aesthetic procedures including peels, lasers, and injectables. **Regulatory status:** - CE-marked **Clinician FAQs:** **What results can patients expect from mesohyal treatments and are they safe?** Patients typically notice improved skin hydration, firmness, and radiance within 2–3 sessions, with optimal results after a full protocol of 4–6 sessions spaced 7–14 days apart. mesohyal formulations use non-crosslinked hyaluronic acid combined with vitamins, minerals, and amino acids, making them highly biocompatible with minimal risk of adverse reactions. The most common side effects are mild redness or micro-bruising at injection sites, which resolve within 24–48 hours. All mesohyal products are CE-marked medical devices manufactured under strict pharmaceutical-grade standards by mesoestetic. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### mesohyal® **Brand:** MESOESTETIC **Type:** soft_product **Portfolio status:** direct portfolio Intradermal medical solutions for facial and body rejuvenation **Market access:** CE-marked. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: traneX glow **Canonical URL:** https://dubaimed.com/products/tranex-glow **Brand:** MESOESTETIC ### For patients ### traneX glow **Learn more:** https://dubaimed.com/products/tranex-glow Multi step professional depigmentation and radiance treatment **What it treats:** brightening, glow, uneven tone, dull skin, lack of radiance, mild pigmentation, photoaging, skin fatigue, post-treatment maintenance, pigmentation prevention. **Questions patients commonly ask:** **What concerns does traneX glow address?** Hyperpigmentation, uneven tone, dullness, and textural irregularities. **How soon are results visible** Visible improvement typically appears after the first session. **Is the treatment suitable for all skin types?** Yes. Suitability is determined during consultation. **Can traneX glow be combined with other treatments?** Yes. It can complement multiple aesthetic procedures. **What is tranex glow and how does it work?** tranex glow is a brightening skincare line by MESOESTETIC formulated with tranexamic acid to inhibit melanin production, reduce hyperpigmentation, and restore an even, luminous skin tone. **Who should use tranex glow and what conditions does it address?** tranex glow is ideal for those with melasma, dark spots, post-inflammatory hyperpigmentation, and uneven skin tone. It suits all skin types seeking a brighter, more uniform complexion. **How do I use tranex glow products in my skincare routine?** Apply tranex glow serum or cream to clean skin morning and evening. Use sunscreen daily as brightening actives increase sun sensitivity. Consistent use over 8-12 weeks yields best results. **What results can I expect from tranex glow and when?** Visible brightening and reduction in dark spots typically appear within 4-6 weeks of daily use. Continued use delivers progressive improvement in overall skin clarity and radiance. **Is tranex glow safe and are there any side effects?** tranex glow is dermatologically tested and safe for daily use on all skin types. Mild tingling upon initial application is normal. Always pair with SPF to protect brightened skin. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### traneX glow **URL:** https://dubaimed.com/products/tranex-glow **Brand:** MESOESTETIC **Product type:** soft_product **Category:** soft-products **Technical overview:** tranex glow is mesoestetic's advanced brightening and luminosity-restoring skincare line formulated with tranexamic acid as its hero ingredient. Tranexamic acid is a powerful depigmenting and brightening agent that works by inhibiting plasminogen activation in keratinocytes, which in turn reduces melanocyte-stimulating signals and decreases melanin production. The tranex glow line targets dull, fatigued skin lacking radiance, uneven skin tone, early pigmentation irregularities, and photoaged complexion. The range typically includes serums, creams, and concentrated treatments that combine tranexamic acid with complementary brightening and antioxidant actives such as vitamin C, niacinamide, and botanical extracts for a synergistic glow-enhancing effect. Unlike mesoestetic's intensive depigmentation methods (cosmelan, dermamelan), tranex glow is positioned as a daily-use cosmeceutical line for prevention, maintenance, and mild-to-moderate pigmentation concerns. It serves as an excellent complement to professional depigmenting treatments, helping maintain and extend clinical results. The formulations are designed for long-term daily use with high tolerability across all skin types. tranex glow is ideal for patients seeking progressive brightening without the intensity of a professional peel protocol. **Unique features:** Tranexamic acid-based brightening system with a unique mechanism of action — inhibits plasminogen activation to reduce melanocyte-stimulating signals. Daily-use cosmeceutical positioning for prevention and maintenance, complementing mesoestetic's intensive depigmentation protocols (cosmelan/dermamelan). Synergistic formulation combining tranexamic acid with vitamin C, niacinamide, and botanical antioxidants for multi-pathway brightening. High tolerability for long-term daily use across all skin types without irritation. Progressive brightening approach ideal for mild-to-moderate pigmentation and overall radiance restoration. Serves as post-treatment maintenance to extend and sustain professional depigmentation results. Targets both melanin overproduction and oxidative dullness for a comprehensive glow effect. **Clinical indications:** - brightening - glow - uneven tone - dull skin - lack of radiance - mild pigmentation - photoaging - skin fatigue - post-treatment maintenance - pigmentation prevention **Clinician FAQs:** **What makes the protocol unique?** Its three-phase structure and senopeptide® technology support both depigmentation and skin renewal. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### traneX glow **Brand:** MESOESTETIC **Type:** soft_product **Portfolio status:** direct portfolio Multi step professional depigmentation and radiance treatment **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: Viora V Series **Canonical URL:** https://dubaimed.com/products/viora-v-series **Brand:** SINCLAIR ### For patients ### Viora V Series **Learn more:** https://dubaimed.com/products/viora-v-series Multi‑technology platform **What it treats:** skin tightening, body contouring, cellulite, skin quality, wrinkle reduction, facial lifting, circumferential reduction, acne treatment, skin texture, lymphatic drainage. **Regulatory status:** FDA-cleared. **Questions patients commonly ask:** **Are all patients suitable for V Series treatments?** No. Candidacy depends on skin type, medical history, treatment area, and the handpiece being considered. A practitioner review is required before treatment. **How does the IPL component treat pigmentation and vessels** V‑IPL emits filtered light that is absorbed by specific chromophores such as melanin or hemoglobin. The absorbed energy converts to heat inside the target, which can lead to its controlled breakdown while sparing surrounding structures when parameters are correctly selected. **What is the role of the fractional RF handpiece** V‑FR creates a pattern of micro‑ablative and coagulation zones while keeping surrounding tissue intact. This stimulates a repair response that can refine texture, reduce the appearance of scars, and smooth the skin surface. **Can the Nd:YAG handpiece be used on darker skin types** Yes. The 1064 nm wavelength travels deeper and is less absorbed by epidermal melanin, which makes it suitable for higher Fitzpatrick phototypes when used with appropriate settings and clinical judgement. **What is Viora V Series and how does it work?** Viora V Series is a multi-technology RF platform by SINCLAIR that uses radiofrequency, vacuum, and LED to deliver skin tightening, body contouring, and facial rejuvenation treatments. **What conditions can Viora V Series treat?** Viora V Series treats skin laxity, wrinkles, cellulite, localized fat, acne, and uneven skin texture. Its modular design allows customized face and body treatments. **What is the treatment process with Viora V Series?** The practitioner selects the appropriate handpiece and energy mode for the target concern. Treatment involves controlled RF energy delivery with real-time monitoring. Sessions last 20-45 minutes. **What results does Viora V Series deliver and what is the downtime?** Patients notice firmer, smoother skin after 3-6 sessions. Skin tightening continues to improve over weeks as collagen rebuilds. Downtime is minimal with only mild redness post-treatment. **Is Viora V Series safe and what side effects should I expect?** Viora V Series is FDA-cleared with built-in safety controls including real-time temperature monitoring. Side effects are minimal — temporary warmth, mild redness, or slight swelling may occur. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Viora V Series **URL:** https://dubaimed.com/products/viora-v-series **Brand:** SINCLAIR **Product type:** medical_device **Category:** medical-devices **Technical overview:** Viora V Series is a versatile multi-technology aesthetic platform manufactured by Viora (now under Sinclair Pharma) that combines multiple energy modalities in a single system for comprehensive non-invasive face and body treatments. The platform integrates advanced radiofrequency (RF) technology, including multi-frequency RF with switchable frequencies, infrared light, vacuum suction, and LED therapy to address a wide range of aesthetic concerns. The V Series is built on Viora's proprietary CORE (Channeling Optimized RF Energy) technology, which uses multi-channel RF delivery to selectively target different tissue depths and achieve precise thermal effects. Clinical applications include facial skin tightening and lifting, body contouring and circumferential reduction, cellulite treatment and improvement, wrinkle reduction, acne treatment, skin texture and tone improvement, and post-treatment recovery support. The system's modular design allows clinics to configure multiple handpieces and applicators for different treatment protocols, making it a cost-effective all-in-one solution that can replace several standalone devices. **Unique features:** Viora V Series is built on proprietary CORE (Channeling Optimized RF Energy) technology that delivers multi-channel radiofrequency energy at switchable frequencies, enabling practitioners to selectively target superficial, mid, and deep tissue layers within a single treatment session. The platform combines four energy modalities — RF, infrared, vacuum, and LED — providing unmatched treatment versatility from a single device. The multi-frequency RF capability allows real-time switching between frequencies to optimize energy delivery for different tissue types and treatment depths. The vacuum-assisted RF handpieces improve energy coupling with the skin, enhance blood circulation, and facilitate lymphatic drainage for superior body contouring results. Built-in temperature monitoring with real-time feedback ensures consistent, safe energy delivery while protecting the epidermis. The modular system architecture supports interchangeable applicators, allowing clinics to expand treatment offerings without purchasing additional platforms. **Clinical indications:** - skin tightening - body contouring - cellulite - skin quality - wrinkle reduction - facial lifting - circumferential reduction - acne treatment - skin texture - lymphatic drainage **Regulatory status:** - FDA-cleared **Positioning:** Also known as: Volnewmer. Compared against: radiofrequency body contouring. **Clinician FAQs:** **How do the RF handpieces work?** V‑FORM, V‑FC, and V‑ST pass bi‑polar RF current through the tissue, generating heat in the dermis and subcutaneous layers. This thermal effect is used for collagen remodelling, tightening, or circumferential reduction, depending on the protocol. **Can the Nd:YAG handpiece be used on darker skin types** Yes. The 1064 nm wavelength travels deeper and is less absorbed by epidermal melanin, which makes it suitable for higher Fitzpatrick phototypes when used with appropriate settings and clinical judgement. **Is Viora V Series safe and what side effects should I expect?** Viora V Series is FDA-cleared with built-in safety controls including real-time temperature monitoring. Side effects are minimal — temporary warmth, mild redness, or slight swelling may occur. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Viora V Series **Brand:** SINCLAIR **Type:** medical_device **Portfolio status:** direct portfolio Multi‑technology platform **Market access:** FDA-cleared. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: AnteAGE® MDX Exosome **Canonical URL:** https://dubaimed.com/products/anteage-mdx-exosome **Brand:** AnteAGE ### For patients ### AnteAGE® MDX Exosome **Learn more:** https://dubaimed.com/products/anteage-mdx-exosome Pure Exosomes Solution contains purified bone marrow stem cell exosomes **What it treats:** anti-aging, skin regeneration, collagen production, elastin production, wound healing, post-laser recovery, post-RF recovery, post-procedure amplification, skin rejuvenation, wrinkle reduction, skin texture improvement, fine lines, skin laxity, inflammation control, cellular repair. **Questions patients commonly ask:** **What is ANTEAGE® MDX EXOSOME?** ANTEAGE® MDX EXOSOME is a professional-grade regenerative skincare solution containing authentic exosomes derived from human bone marrow mesenchymal stem cells. These natural nanoparticles deliver over 300 growth factors and signaling molecules to support comprehensive skin rejuvenation, repair, and anti-aging. **How do natural exosomes differ from synthetic Biosomes™?** Natural exosomes from BMSC contain the complete biological complexity of stem cell signaling, including hundreds of naturally occurring growth factors, cytokines, and microRNAs. This comprehensive profile provides broad-spectrum regenerative benefits. Synthetic Biosomes™ offer consistency and specific targeted action with selected molecules, providing a controlled approach for particular concerns. **What makes BMSC exosomes special?** Bone marrow mesenchymal stem cells are known for their exceptional regenerative capacity and anti-inflammatory properties. Exosomes derived from these cells carry the same regenerative intelligence, making them particularly effective for tissue repair, collagen production, and cellular rejuvenation in skin applications. **Is ANTEAGE® MDX EXOSOME safe?** Yes. ANTEAGE® MDX EXOSOME undergoes strict quality control and safety testing. The human bone marrow stem cells used are ethically sourced, extensively screened, and cultured under controlled laboratory conditions. The product has established safety across years of clinical use in professional settings. **Which concerns can it address?** ANTEAGE® MDX EXOSOME is effective for anti-aging, wrinkles, skin laxity, post-procedure healing, barrier repair, inflammation, scarring, uneven texture, and hair thinning. Its comprehensive regenerative profile makes it suitable for multiple aesthetic concerns. **What skin conditions does AnteAGE MDX Exosome treat?** Primary indications: - Inflammation control (post-procedure, post-acne, rosacea, irritated skin) - Collagen and elastin rebuilding - Fine lines and wrinkles - Age spots and hyperpigmentation - Skin vitality and luminosity - Brightness, hydration, redness, and skin irritation - Skin lesions and scars (acne, surgical, traumatic) - Skin texture and pore size improvement Post-treatment enhancement (amplifying results of): - Laser resurfacing (CO2, fractional, Er:YAG) - RF microneedling (Secret DUO, Morpheus8) - Dermal microneedling - Chemical peels - IPL/BBL - Any energy-based skin treatment Who benefits most: All skin types, all ages. Especially patients seeking post-procedure acceleration, or those treating scars and hyperpigmentation. **How does AnteAGE MDX Exosome work biologically?** Mechanism step by step: 1. DELIVERY: Exosomes (100nm lipid vesicles) are introduced to skin during or after a procedure. They penetrate easily through micro-channels from needling devices or laser ablation. 2. CELL COMMUNICATION: Exosomes enter neighboring cells without needing a receptor — they merge with the cell membrane and deliver 6,000+ growth factors directly into the cytoplasm. 3. REGENERATIVE CASCADE: Delivered signals (TGF-beta, HGF, KGF, NGF, and many others) trigger: - Collagen synthesis and elastin production - Fibroblast activation - Reduced inflammatory signaling - Reversal of the cellular aging phenotype 4. LASTING EFFECT: Unlike topical GF which sits on the skin surface, exosomes enter the cell and reprogram it — triggering a sustained biological cascade that continues for weeks to months after treatment. **How should AnteAGE MDX Exosome be stored?** Storage requirements: - Refrigerate between 2°C and 8°C (35.6°F–46.4°F) at all times - Do NOT freeze - Protect from direct sunlight and UV exposure - Once opened, use immediately — do not store reconstituted solution Unlike AnteAGE MDX Biosome (room temperature stable), the real exosomes in MDX Exosome are biological materials that require cold chain because they degrade at room temperature over time. In clinic: Store in standard medical refrigerator. Remove immediately before use. Can be briefly warmed in hand before application for patient comfort. Shipping: DUBIMED ships all AnteAGE MDX Exosome products with cold chain packaging to maintain 2°C–8°C during transit. **What results can patients expect from AnteAGE MDX Exosome?** Clinically documented results: After 2 treatments (4–5 months): - Significant reduction in active acne and post-acne scarring - Marked improvement in skin texture and brightness - Visible reduction in hyperpigmentation and sun damage After 3 treatments (3 months): - Dramatic wrinkle reduction and skin tightening - Collagen and elastin rebuilding visible in photographic documentation - Skin texture, pore size, and luminosity markedly improved General clinical data: - 500% increase in collagen and elastin production (in vitro) - 300% more potent than standard AnteAGE GF solution - Results begin immediately after first session - Maximum results continue developing 3–6 months after each treatment - All skin types, all ages Best practice: Series of 2–3 treatments, 4–6 weeks apart, combined with an in-clinic device. Single treatment already delivers meaningful improvement; 2–3 produce transformative results. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### AnteAGE® MDX Exosome **URL:** https://dubaimed.com/products/anteage-mdx-exosome **Brand:** AnteAGE **Product type:** soft-product **Category:** soft-products **Technical overview:** AnteAGE MDX Exosome Solution is the world's most advanced real exosome treatment — the only professional exosome product sourced exclusively from Bone Marrow Mesenchymal Stem Cells (BM-MSCs). Developed by Cellese Biological Lab (USA) and distributed in the Middle East exclusively by DUBIMED. WHAT ARE ANTEAGE MDX EXOSOMES? Exosomes are naturally occurring extracellular vesicles — tiny packages of biosignals produced by stem cells when they sense injury or malfunction. They communicate with neighboring cells to direct healing, control inflammation, and reverse the aging phenotype of the skin. AnteAGE carefully sorts and preserves these exosomes from Bone Marrow Stem Cell culture to deliver maximum therapeutic benefit. KEY SPECIFICATIONS: - 5 Billion Exosome Nanospheres per treatment (5 × 2mL vials) - 100 nm Diameter (independently verified by QNANO, Irvine USA) - 6,000 Unique Growth Factors per vial - Low Molecular Weight HA 150KD (carrier + penetration enhancer) - Zero allergens - 300% more potent than standard AnteAGE MD Growth Factor Solution - 500% increase in collagen and elastin production vs. control - The only exosome from Bone Marrow Stem Cells in the world - 99% purity — no chemical additives - Refrigerate 2°C–8°C | Do NOT freeze - GMP Certified | ISO 7 Clean Room | EUIPO Registered | California State Seal SURFACE MARKER ANALYSIS (MFI study): AnteAGE MDX shows high Medium Fluorescence Intensity for CD9, CD63, and CD81 — the three definitive exosome protein markers. Competitor products independently tested showed NO expression of these vital markers (i.e., they contain no real exosomes). INDEPENDENT PARTICLE ANALYSIS: QNANO (Irvine, USA) confirmed AnteAGE MDX Exosomes register at exactly 100nm — the correct size for real exosomes. A popular competitor product claiming to contain exosomes was found to contain no complete exosomes at all. **Unique features:** 1. THE ONLY EXOSOME IN THE WORLD FROM BONE MARROW STEM CELLS: AnteAGE uses exclusively Bone Marrow Mesenchymal Stem Cell (BM-MSC) secretome — cited by thousands of published studies as the optimal source for skin regeneration. With 11 years of BM-MSC culturing experience, no other aesthetic exosome company has deeper expertise. Result: 6,000 unique growth factors per vial. 2. VERIFIED REAL EXOSOMES — INDEPENDENT PARTICLE ANALYSIS: QNANO (Irvine, USA) confirms AnteAGE MDX Exosomes at exactly 100nm. Surface Marker Analysis (MFI) confirms high CD9, CD63, CD81 expression. A popular competitor independently tested showed no complete exosomes at all. 3. 6,000 UNIQUE GROWTH FACTORS — THE MOST COMPLETE REGENERATIVE SIGNAL: No single recombinant GF product can replicate this complexity. This comprehensive signal library addresses virtually every aspect of skin aging and regeneration simultaneously. 4. 300% MORE POTENT THAN STANDARD GROWTH FACTOR SOLUTION: 500% increase in collagen and elastin production vs. control (in vitro). Results begin immediately after the first session and continue developing for 3–6 months. 5. ZERO ALLERGENS: Derived from Bone Marrow Stem Cells (not PRP, not plant cells, not fetal bovine serum). Safe for immune-sensitive patients and post-inflammatory or reactive skin. 6. PERFECT SYNERGY WITH ENERGY-BASED DEVICES: Exosomes are a natural "damage response" molecule. Applying MDX Exosomes immediately after laser, RF microneedling, or any energy-based treatment creates an amplified healing cascade — dramatically improving outcomes and reducing recovery time. **Clinical indications:** - anti-aging - skin regeneration - collagen production - elastin production - wound healing - post-laser recovery - post-RF recovery - post-procedure amplification - skin rejuvenation - wrinkle reduction - skin texture improvement - fine lines - skin laxity - inflammation control - cellular repair **Clinician FAQs:** **How should it be used?** ANTEAGE® MDX EXOSOME can be applied topically after microneedling, used following laser or RF treatments, or incorporated into professional facial protocols. Application method depends on treatment goals and should be determined by trained practitioners. **Can both ANTEAGE® products be used together?** Yes. Some practices use ANTEAGE® MDX EXOSOME for deep regenerative treatments and ANTEAGE® MDX BIOSOME™ for consistent daily maintenance, combining the strengths of both technologies for comprehensive patient care. **What is AnteAGE MDX Exosome Solution?** AnteAGE MDX Exosome Solution is the world's most advanced real exosome treatment — the only professional exosome product derived exclusively from Bone Marrow Mesenchymal Stem Cells (BM-MSCs). It contains over 5 Billion real Exosome Nanospheres per treatment (5 × 2mL vials), along with more than 6,000 unique growth factors, cytokines, and biological signals. Key specs: - 5 Billion real exosomes per treatment | 100nm diameter - 6,000 unique growth factors per vial - Low Molecular Weight HA 150KD carrier - 300% more potent than standard AnteAGE GF Solution - 500% increase in collagen and elastin (in vitro) - Zero allergens | 99% purity - Refrigerated 2°C–8°C Manufactured by Cellese Biological Lab (USA), ISO 7 Clean Room, GMP Certified. Distributed in the Middle East exclusively by DUBIMED. **What results can patients expect from AnteAGE MDX Exosome?** Clinically documented results: After 2 treatments (4–5 months): - Significant reduction in active acne and post-acne scarring - Marked improvement in skin texture and brightness - Visible reduction in hyperpigmentation and sun damage After 3 treatments (3 months): - Dramatic wrinkle reduction and skin tightening - Collagen and elastin rebuilding visible in photographic documentation - Skin texture, pore size, and luminosity markedly improved General clinical data: - 500% increase in collagen and elastin production (in vitro) - 300% more potent than standard AnteAGE GF solution - Results begin immediately after first session - Maximum results continue developing 3–6 months after each treatment - All skin types, all ages Best practice: Series of 2–3 treatments, 4–6 weeks apart, combined with an in-clinic device. Single treatment already delivers meaningful improvement; 2–3 produce transformative results. **Are AnteAGE MDX Exosomes real exosomes or synthetic?** AnteAGE MDX Exosomes are REAL exosomes — not synthetic, not mimics. They are genuine extracellular vesicles isolated from the conditioned medium of cultured Bone Marrow Mesenchymal Stem Cells (BM-MSCs): 1. BM-MSCs are cultured in Cellese's ISO 7 Clean Room 2. Cells secrete exosomes into the culture medium 3. Exosomes are sorted, purified to 99% purity, and preserved 4. Final product: >5 Billion real exosomes per 2mL vial Independent verification: - QNANO (Irvine, USA): Confirmed at exactly 100nm (correct size for real exosomes) - Surface Marker Analysis (MFI): High expression of CD9, CD63, CD81 — the three definitive exosome protein markers - Competitor test: A popular product claiming to be exosome was independently tested and found to contain NO complete exosomes Compare to Biosome: Biosome uses synthetic lipid nanoparticles engineered to mimic exosomes. Both effective — Exosome offers biological authenticity with 6,000 natural GFs; Biosome offers stability and 5x more particles. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### AnteAGE® MDX Exosome **Brand:** AnteAGE **Type:** soft-product **Portfolio status:** direct portfolio Pure Exosomes Solution contains purified bone marrow stem cell exosomes **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **What is AnteAGE MDX Exosome Solution?** AnteAGE MDX Exosome Solution is the world's most advanced real exosome treatment — the only professional exosome product derived exclusively from Bone Marrow Mesenchymal Stem Cells (BM-MSCs). It contains over 5 Billion real Exosome Nanospheres per treatment (5 × 2mL vials), along with more than 6,000 unique growth factors, cytokines, and biological signals. Key specs: - 5 Billion real exosomes per treatment | 100nm diameter - 6,000 unique growth factors per vial - Low Molecular Weight HA 150KD carrier - 300% more potent than standard AnteAGE GF Solution - 500% increase in collagen and elastin (in vitro) - Zero allergens | 99% purity - Refrigerated 2°C–8°C Manufactured by Cellese Biological Lab (USA), ISO 7 Clean Room, GMP Certified. Distributed in the Middle East exclusively by DUBIMED. ## Product: SkinPen® **Canonical URL:** https://dubaimed.com/products/skinpen **Brand:** REVANCE ### For patients ### SkinPen® **Learn more:** https://dubaimed.com/products/skinpen FDA‑cleared microneedling device **What it treats:** acne scars, facial acne scars, surgical scars, neck wrinkles, fine lines, wrinkles, stretch marks, skin texture, skin tone, pore size, hyperpigmentation, hypopigmentation, dyschromia, skin rejuvenation, collagen stimulation, elastin production, product absorption. **Regulatory status:** FDA-cleared. **Questions patients commonly ask:** **How many treatments are required?** Treatment frequency varies by indication. Most protocols involve multiple sessions spaced several weeks apart, determined by practitioner assessment. **Is there downtime?** Downtime is generally minimal. Temporary erythema or sensitivity may occur and typically resolves within a short period. **Is SkinPen suitable for all skin types?** Yes. The device is appropriate for all Fitzpatrick skin types and can be used year‑round under professional supervision. **How does SkinPen works?** SkinPen creates controlled microchannels that activate the body’s wound‑healing response. This process supports collagen and elastin production, improving texture and reducing the appearance of wrinkles and scars. **What conditions does SkinPen treat and who is it suitable for?** SkinPen holds FDA clearance for two specific indications: facial acne scars in adults aged 22+ (all skin types, Fitzpatrick I-VI) and neck wrinkles (Fitzpatrick II-IV). Beyond these cleared indications, practitioners use SkinPen for fine lines and wrinkles, stretch marks, enlarged pores, uneven skin texture and tone, hyperpigmentation, surgical scars, and overall skin rejuvenation. It is safe for all skin types and tones year-round, with no seasonal restrictions — unlike laser and chemical treatments that carry hyperpigmentation risks for darker skin tones. **What results can I expect and how much downtime is there?** Clinical trials show 90% of patients recommend SkinPen at both 1 month and 6 months post-treatment, with 85% reporting satisfaction. For neck wrinkles specifically, 94% saw improvement at 1 month. Results begin appearing after the first session and continue improving for 3-6 months after the last treatment as new collagen and elastin form. Downtime is minimal — skin appears red and flushed (similar to a mild sunburn) with possible tightness and mild sensitivity. This typically resolves within 24-72 hours. Makeup and sunscreen can be applied 24 hours post-treatment. After 3 days, there is rarely visible evidence that the procedure took place. **Is SkinPen safe? What are the contraindications and side effects?** SkinPen Precision is backed by over 90 validation studies and has treated more than 3 million patients worldwide. Its BioSheath technology prevents cross-contamination between patients, and AAVS technology ensures perpendicular needle entry to minimize epidermal tearing. Side effects are mild and temporary: redness, skin tightness, mild sensitivity, dryness, and occasional peeling — all typically resolving within 24-72 hours. SkinPen should NOT be used on patients with: active skin cancer in the treatment area, open wounds or irritated skin, allergy to stainless steel or anesthetics, bleeding disorders, pregnancy or nursing, or current isotretinoin (Accutane) use. The device should not be used within the orbital rim (eyelids), and safety above 1.5mm depth has not been formally evaluated. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### SkinPen® **URL:** https://dubaimed.com/products/skinpen **Brand:** REVANCE **Product type:** medical_device **Category:** medical-devices **Technical overview:** SkinPen Precision is the first FDA-cleared microneedling device in the world — a precision-engineered skin remodeling system that uses collagen induction therapy (CIT) to trigger the body's natural wound healing response, producing new collagen and elastin for visibly healthier, more youthful skin. Originally developed by Bellus Medical, SkinPen became part of Crown Aesthetics and is now under Revance Therapeutics. DUBIMED is the official distributor for UAE, Qatar, and Oman. The device creates thousands of controlled micro-channels in the skin using a single-use sterile cartridge with 14 surgical-grade stainless steel needles at adjustable depths from 0.25mm to 2.5mm. This triggers a three-phase healing cascade: Inflammation (clean wound, increase blood flow), Proliferation (rebuild with new granulation cells), and Remodeling (new dermal tissue and blood supply form, producing collagen and elastin). No chemicals, no heat, no invasive injections. FDA CLEARANCES: - De Novo Classification DEN160029 (Class II): Treatment of facial acne scars in adults aged 22+, all Fitzpatrick skin types - 510(k) K202243: Treatment of neck wrinkles, Fitzpatrick skin types II-IV The latest SkinPen Precision Elite model delivers 7,000 RPM motor speed, places over 1,600 controlled micro-injuries per second (approximately 3 million per 30-minute procedure), and features needle sharpness validated for up to 80 minutes of continuous use. CLINICAL RESULTS (from clinical trials): - 90% of patients recommend SkinPen to family and friends at 1 month and 6 months - 85% patient satisfaction at 1 month and 6 months - 94% of patients saw improvement in neck wrinkles at 1 month post-treatment - Over 90 validation studies for quality, safety, and performance - Over 3 million patients treated worldwide - More providers use SkinPen than any other microneedling brand (10,000+ providers in the US alone) TREATMENT PROTOCOL: - Session duration: 30-60 minutes depending on area - Recommended: 3-4+ sessions spaced 30 days apart - Pre-treatment: gentle cleansing, LIFT Hydrogel application, topical anesthetic for comfort - Post-treatment: Skinfuse 90-day post-procedure protocol for optimal results - Downtime: minimal — redness similar to mild sunburn, typically resolves within 24-72 hours - Makeup and sunscreen permitted 24 hours post-treatment - Skin improvements continue for 3-6 months following last treatment AWARDS: Aesthetic Guide 2022 Best in Industry, NewBeauty Award Winner 2022, Cosmopolitan Beauty Award, Medical Beauty Gold Award. CONTRAINDICATIONS: Active skin cancer in treatment area, open wounds/sores, allergy to stainless steel or anesthetics, hemorrhagic/hemostatic disorders, pregnancy or nursing, current isotretinoin (Accutane) use. Not for use within the orbital rim (eyelids). Safety above 1.5mm depth not formally evaluated. **Unique features:** 1. FIRST FDA-CLEARED MICRONEEDLING DEVICE: SkinPen Precision is the only microneedling device with two FDA clearances — De Novo DEN160029 for facial acne scars (all Fitzpatrick skin types, aged 22+) and 510(k) K202243 for neck wrinkles (Fitzpatrick II-IV). No other microneedling device matches this regulatory validation. 2. BIOSHEATH CROSS-CONTAMINATION PREVENTION: Proprietary BioSheath technology creates a physical barrier between the sterile needle cartridge and the device body, preventing biological fluid backflow into the motor housing. This eliminates the cross-contamination risk present in devices without such barriers. 3. AAVS (ADVANCED AUTO-ADJUSTING VERTICAL STAMP) TECHNOLOGY: Ensures perpendicular needle entry at every angle regardless of the practitioner's hand position, minimizing epidermal tearing and reducing patient discomfort compared to devices with angled needle penetration. 4. PRECISION ELITE PERFORMANCE: The latest model operates at 7,000 RPM (±700), placing over 1,600 controlled micro-injuries per second — approximately 3 million per 30-minute procedure. Needle sharpness validated for up to 80 minutes of continuous use, allowing treatment of multiple areas with one cartridge. 5. 14-NEEDLE SURGICAL-GRADE CARTRIDGE: Single-use sterile cartridge with 14 surgical-grade stainless steel needles. Adjustable depth from 0.25mm to 2.5mm in precise increments for treatment customization across facial zones, neck, and body areas. 6. CLINICALLY PROVEN OUTCOMES: 90+ validation studies. 90% patient recommendation rate at 6 months. 94% saw neck wrinkle improvement at 1 month. Over 3 million patients treated. More providers use SkinPen than any other microneedling brand. 7. SKINFUSE 90-DAY POST-PROCEDURE PROTOCOL: Dedicated post-treatment product series formulated to support skin healing and maximize collagen production following microneedling — extending clinical results beyond the treatment session. 8. ALL SKIN TYPES, YEAR-ROUND: Safe for all Fitzpatrick skin types (I-VI for acne scars), with no seasonal restrictions. No chemicals, no heat — purely mechanical collagen induction eliminates the risk of post-inflammatory hyperpigmentation associated with thermal or chemical treatments. 9. DESIGNED AND MANUFACTURED IN NORTH AMERICA: Engineered, manufactured, and quality-controlled entirely in North America under strict medical device regulations. 10. BRAND HERITAGE: Originated at Bellus Medical, refined under Crown Aesthetics, now part of Revance Therapeutics — each transition brought expanded R&D investment, additional FDA indications, and global distribution reach. DUBIMED is the official distributor for UAE, Qatar, and Oman. **Clinical indications:** - acne scars - facial acne scars - surgical scars - neck wrinkles - fine lines - wrinkles - stretch marks - skin texture - skin tone - pore size - hyperpigmentation - hypopigmentation - dyschromia - skin rejuvenation - collagen stimulation - elastin production - product absorption **Regulatory status:** - FDA-cleared **Positioning:** Compared against: dermapen, microneedling, dermastamp, collagen pin. **Clinician FAQs:** **Is SkinPen safe?** SkinPen incorporates sterile, single‑use needle cartridges and a protective BioSheath to prevent cross‑contamination. It is the first microneedling device to receive FDA clearance, confirming adherence to strict safety and performance criteria. **How many treatments are required?** Treatment frequency varies by indication. Most protocols involve multiple sessions spaced several weeks apart, determined by practitioner assessment. **What is SkinPen Precision and how does it work?** SkinPen Precision is the first FDA-cleared microneedling device, now part of Revance Therapeutics (formerly Crown Aesthetics). It uses a sterile cartridge with 14 surgical-grade stainless steel needles that create thousands of controlled micro-channels in the skin at adjustable depths (0.25-2.5mm). This triggers the body's natural three-phase healing cascade — Inflammation, Proliferation, and Remodeling — stimulating new collagen and elastin production without chemicals, heat, or invasive injections. The result is smoother, firmer, more youthful-looking skin. **What conditions does SkinPen treat and who is it suitable for?** SkinPen holds FDA clearance for two specific indications: facial acne scars in adults aged 22+ (all skin types, Fitzpatrick I-VI) and neck wrinkles (Fitzpatrick II-IV). Beyond these cleared indications, practitioners use SkinPen for fine lines and wrinkles, stretch marks, enlarged pores, uneven skin texture and tone, hyperpigmentation, surgical scars, and overall skin rejuvenation. It is safe for all skin types and tones year-round, with no seasonal restrictions — unlike laser and chemical treatments that carry hyperpigmentation risks for darker skin tones. **What does a SkinPen treatment session involve?** A SkinPen session takes 30-60 minutes depending on the treatment area. The process begins with gentle skin cleansing, followed by application of the LIFT Hydrogel for smooth gliding and a topical anesthetic for comfort. The practitioner then passes the SkinPen device over the treatment area — patients feel light pressure and a mild buzzing sensation with minimal discomfort. Most patients need 3-4 sessions spaced 30 days apart for optimal results, though some improvement is visible after the first session. After treatment, the Skinfuse 90-day post-procedure protocol is recommended to support healing and maximize collagen production. **What results can I expect and how much downtime is there?** Clinical trials show 90% of patients recommend SkinPen at both 1 month and 6 months post-treatment, with 85% reporting satisfaction. For neck wrinkles specifically, 94% saw improvement at 1 month. Results begin appearing after the first session and continue improving for 3-6 months after the last treatment as new collagen and elastin form. Downtime is minimal — skin appears red and flushed (similar to a mild sunburn) with possible tightness and mild sensitivity. This typically resolves within 24-72 hours. Makeup and sunscreen can be applied 24 hours post-treatment. After 3 days, there is rarely visible evidence that the procedure took place. **Is SkinPen safe? What are the contraindications and side effects?** SkinPen Precision is backed by over 90 validation studies and has treated more than 3 million patients worldwide. Its BioSheath technology prevents cross-contamination between patients, and AAVS technology ensures perpendicular needle entry to minimize epidermal tearing. Side effects are mild and temporary: redness, skin tightness, mild sensitivity, dryness, and occasional peeling — all typically resolving within 24-72 hours. SkinPen should NOT be used on patients with: active skin cancer in the treatment area, open wounds or irritated skin, allergy to stainless steel or anesthetics, bleeding disorders, pregnancy or nursing, or current isotretinoin (Accutane) use. The device should not be used within the orbital rim (eyelids), and safety above 1.5mm depth has not been formally evaluated. **What makes SkinPen different from other microneedling devices?** SkinPen is the only microneedling brand with two FDA clearances (acne scars + neck wrinkles), giving it regulatory credibility no competitor matches. Its BioSheath technology is unique — most microneedling pens lack a physical barrier preventing biological fluid backflow into the motor, creating cross-contamination risk. The AAVS technology ensures perpendicular needle entry regardless of hand angle, which reduces epidermal tearing compared to devices with angled penetration. The Precision Elite model's 7,000 RPM motor and 80-minute needle validation allow treatment of multiple areas per cartridge. SkinPen also offers the Skinfuse 90-day post-procedure protocol — a dedicated aftercare system that most competitors lack. With over 3 million patients treated and 90+ validation studies, SkinPen has the deepest clinical evidence base of any microneedling device. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### SkinPen® **Brand:** REVANCE **Type:** medical_device **Portfolio status:** direct portfolio FDA‑cleared microneedling device **Market access:** FDA-cleared. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: AnteAGE® MD **Canonical URL:** https://dubaimed.com/products/anteage-md **Brand:** AnteAGE ### For patients ### AnteAGE® MD **Learn more:** https://dubaimed.com/products/anteage-md Bone marrow–derived growth factors and cytokines for professional skin rejuvenation **What it treats:** anti-aging, collagen stimulation, elastin production, wrinkle reduction, skin tightening, skin texture improvement, hyperpigmentation, melasma, age spots, uneven skin tone, hair loss, hair thinning, follicle reactivation, post-microneedling recovery, skin rejuvenation. **Questions patients commonly ask:** **Can AnteAGE MD Skin be used at home?** Home‑use versions exist, but the MD formulation is strictly for professional application. **How long until results appear?** Visible improvements typically develop within several weeks, with continued enhancement over multiple sessions. **What are the indications for AnteAGE MD Skin?** It is indicated for aging skin, fine lines, wrinkles, redness, texture irregularities, and post‑procedure recovery. **What is the difference between the AnteAGE MD Microneedling Treatment and the AnteAGE MD Brightner solution?** AnteAGE MD Microneedling solution is designed to enhance the results of microneedling treatments, while the AnteAGE MD Brightener solution is designed to reduce the appearance of hyperpigmentation and even out skin tone. Each product has its own unique blend of ingredients and is designed to be used for different purposes. **What does the AnteAGE MD Skin System include and how is it used?** IN-CLINIC (Professional Use Only): AnteAGE MD® Microneedling Solution: Contains pro-healing, anti-inflammatory growth factors, cytokines, antioxidants, and hyaluronic acid. Applied during precision needling (derma stamper, derma roller, micropin). The needling device creates micro-channels — the brain amplifies the healing response and AnteAGE MD supercharges it with growth factors. HOME — STEP 1 (AM/PM): AnteAGE MD® Serum (GF | Serum 30mL): High concentration GF + cytokines. Nanotechnology for rapid penetration to deepest skin layers. Optimizes tone and texture. Massage 2–3 pumps into face and neck until absorbed. HOME — STEP 2 (AM/PM, after Serum): AnteAGE MD® Accelerator (GF | Accelerator 30mL): Cytokines + vitamins + targeted antioxidants. Deep hydration + pro-healing anti-inflammatory effect. Massage 2–3 pumps. Recommended at night for sensitive skin. Expected results: - Initial: Within first week of complete system use - Final: Visible after 6 weeks - Brightening + lifting | Pore minimizing | Skin tightening | Inflammation reduction | Fine line and wrinkle reduction | Prevents new signs of aging **How does the AnteAGE MD Brightening System treat pigmentation?** The AnteAGE MD Brightening System fades discoloration without drying, irritation, or inflammation: Key ingredients: - Tranexamic acid: Reduces melanocyte-keratinocyte interaction → directly reduces melanin production; inhibits tyrosinase enzyme - Engineered peptides: Inhibit multiple stages of the pigmentation cascade - Growth factors + cytokines: Stimulate healthy cell renewal, replacing pigmented cells with new keratinocytes - No hydroquinone, no harsh bleaching agents Indications: - Hyperpigmentation (all types) - Melasma - Age spots and liver spots - Sun damage - Post-inflammatory hyperpigmentation (PIH) - Uneven skin tone Application: Microneedling solution — applied during in-clinic needling procedure. Micro-channels allow brightening actives to penetrate deep into the dermis where pigmentation originates. Clinical results: Visible brightening at 60 days. Specs: 2mL unit doses | Paraben-Free | Dye-Free | Cruelty-Free | Made in USA **When do AnteAGE MD results appear and how long do they last?** Complete system timeline (in-clinic + Serum + Accelerator): - Initial results: Within the first week of complete system use - Final outcomes: Visible after 6 weeks of consistent use - Hair results: Visible within 8–12 weeks; significant improvement after 2–5 treatments - Brightening results: Visible at 60 days Expected clinical improvements: - Visible brightening and lifting effect - Pore minimization - Skin tightening - Reduced inflammation - Reduced redness and blemishes - Fine line and wrinkle reduction - Prevention of new visible aging signs Maintenance: Sustained with daily Serum + Accelerator use and periodic in-clinic maintenance (typically every 3–6 months). **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### AnteAGE® MD **URL:** https://dubaimed.com/products/anteage-md **Brand:** AnteAGE **Product type:** soft-product **Category:** soft-products **Technical overview:** AnteAGE MD is the professional in-clinic treatment line from AnteAGE — growth factor and cytokine-powered microneedling solutions designed to work with precision needling devices (derma stamper, derma roller, micropin) and energy-based treatments. Manufactured by Cellese Biological Lab (USA) and distributed in the Middle East exclusively by DUBIMED. THE SCIENCE: As we age, skin loses its growth factor and cytokine concentration — the biosignals that allow skin to repair and renew itself. AnteAGE MD restores these signals with 20+ clinically active ingredients, directly supporting the skin's natural healing cascade during in-clinic procedures. THREE CLINICAL SYSTEMS: 1. ANTEAGE MD SKIN SYSTEM: - AnteAGE MD® Microneedling Solution (In-Clinic, Professional Use Only): Pro-healing, anti-inflammatory growth factors + cytokines + antioxidants + hyaluronic acid. The doctor creates micro-channels with the needling device while the solution is on the skin — the brain interprets these as wounds and amplifies the healing response, supercharged by the growth factors in the solution. - AnteAGE MD® Serum (Home Step 1, 30mL): High concentration GF + cytokines. Nanotechnology for rapid deep absorption. Optimizes tone, texture, nourishment. AM/PM: massage 2–3 pumps. - AnteAGE MD® Accelerator (Home Step 2, 30mL): Cytokines + vitamins + antioxidants. Deep hydration + anti-inflammatory. AM/PM after Serum. Night use recommended for sensitive skin. Results: Initial within week 1; final after 6 weeks (complete system). 2. ANTEAGE MD BRIGHTENING SYSTEM: - Brightening Microneedling Solution: Tranexamic acid + engineered peptides + GF for pigmentation fading without drying or irritation. - Targets: Hyperpigmentation, melasma, age spots, sun damage, uneven skin tone. - Paraben-Free | Dye-Free | Cruelty-Free | Made in USA - Documented: Visible brightening at 60 days. 3. ANTEAGE MD HAIR SYSTEM: - Designed to awaken dormant hair follicle stem cells via WNT1 Stem Cytokines™ + natural stimulants. - Clinical treatment: Micro-needles deliver growth factors directly to hair follicles, stimulating reactivation. Protects healthy follicles. Best results after 5 in-office treatments. - Clinical study (28 participants, 12 weeks): 82% major improvement in hair loss; 50% new hair growth. - Results visible: 8–12 weeks. - Combines with AnteAGE MD® in-office hair microneedling for amplified results. **Unique features:** 1. 20+ CLINICALLY ACTIVE INGREDIENTS IN ONE SYSTEM: More than 20 clinically proven active ingredients per treatment — GF, cytokines, antioxidants, HA, and targeted actives working synergistically at the cellular level. 2. ENGINEERED FOR PRECISION NEEDLING: Specifically formulated to work with derma stampers, rollers, and micropins. As needles create micro-channels, the solution penetrates to the dermis where regenerative signals are needed most. The needles amplify the brain's repair response — AnteAGE MD amplifies that response further. 3. COMPLETE IN-CLINIC + HOME CONTINUUM: - In-clinic: Microneedling Solution (professional only) - Home Step 1: Serum (AM/PM, nano-enhanced absorption) - Home Step 2: Accelerator (AM/PM, cytokine moisturizer) The complete system delivers initial results within 1 week and sustained long-term outcomes. 4. THREE TARGETED SYSTEMS FOR DIFFERENT CONCERNS: - Skin System: Anti-aging, collagen, elastin, tightening, wrinkle reduction - Brightening System: Tranexamic acid + peptides for hyperpigmentation/melasma - Hair System: WNT1 Stem Cytokines for follicle stem cell activation 5. HAIR SYSTEM CLINICAL EVIDENCE (28 participants, 12 weeks): - 82% major improvement in hair loss - 50% new hair growth - Best results after 5 in-office treatments WNT1 Stem Cytokines are the key signaling molecule for hair follicle stem cell activation — more targeted than PRP. **Clinical indications:** - anti-aging - collagen stimulation - elastin production - wrinkle reduction - skin tightening - skin texture improvement - hyperpigmentation - melasma - age spots - uneven skin tone - hair loss - hair thinning - follicle reactivation - post-microneedling recovery - skin rejuvenation **Clinician FAQs:** **Can I use AnteAGE MD Skincare at home?** AnteAGE MD Microneedling Treatment is a medical-use-only procedure that should only be performed by certified AnteAGE MD Providers, But there is AnteAGE MD Home Skincare System is designed for daily use at home, **What is AnteAGE MD and how is it different from AnteAGE MDX?** AnteAGE MD is AnteAGE's professional in-clinic treatment line using concentrated growth factors and cytokines derived from Bone Marrow Stem Cells. Specifically formulated for use with microneedling devices, complemented by a home care system (Serum + Accelerator). Key differences: - AnteAGE MD: Growth factor proteins (conditioned media / cytokines). Microneedling-specific. Comes with home Serum + Accelerator for daily use. - AnteAGE MDX Exosome: Complete real Exosomes (6,000 GFs per vial). 300% more potent. Refrigerated. - AnteAGE MDX Biosome: Engineered synthetic Biosomes (25 Billion particles). Room temperature stable. Think of it as a progression: AnteAGE MD is the powerful professional GF foundation. MDX products are the next generation — delivering the complete exosome experience for those requiring maximum regeneration. Available systems: Skin System, Brightening System, Hair System. **How does the AnteAGE MD Hair System treat hair loss?** THE SCIENCE: Every hair follicle has a bulge of stem cells managing growth cycles. With age, growth factor and cytokine signals decline, stem cells become dormant, hair enters prolonged telogen (resting) — visible thinning and loss. AnteAGE MD Hair System: - WNT1 Stem Cytokines™: The WNT signaling pathway is the master regulator of hair follicle stem cell activation. WNT1 cytokines specifically reactivate dormant follicle stem cells and extend the anagen (growth) phase. - Hair Polybotanical: Plant-derived biosignals with clinically proven hair growth activity. - Together: Two-formula system wakes sleeping follicles and returns them to a youthful growth pattern. Clinical treatment: Medical practitioners use micro-needles to deliver growth factors directly to follicles — stimulating reactivation and protecting healthy follicles. Best results after 5 in-office treatments. Clinical study (28 participants, 12 weeks): - 82% major improvement in hair loss - 50% new hair growth - Results visible within 8–12 weeks vs. PRP: AnteAGE Hair System uses a more targeted GF formulation precisely engineered for follicle stimulation — more precise than PRP's broad platelet mix. **When do AnteAGE MD results appear and how long do they last?** Complete system timeline (in-clinic + Serum + Accelerator): - Initial results: Within the first week of complete system use - Final outcomes: Visible after 6 weeks of consistent use - Hair results: Visible within 8–12 weeks; significant improvement after 2–5 treatments - Brightening results: Visible at 60 days Expected clinical improvements: - Visible brightening and lifting effect - Pore minimization - Skin tightening - Reduced inflammation - Reduced redness and blemishes - Fine line and wrinkle reduction - Prevention of new visible aging signs Maintenance: Sustained with daily Serum + Accelerator use and periodic in-clinic maintenance (typically every 3–6 months). **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### AnteAGE® MD **Brand:** AnteAGE **Type:** soft-product **Portfolio status:** direct portfolio Bone marrow–derived growth factors and cytokines for professional skin rejuvenation **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: ZYE **Canonical URL:** https://dubaimed.com/products/zye **Brand:** VYDENCE ### For patients ### ZYE **Learn more:** https://dubaimed.com/products/zye SmartLASER platform for skin rejuvenation and hair removal **What it treats:** aesthetic treatment, clinic technology, hair removal, permanent hair reduction, pseudofolliculitis barbae, ingrown hairs, skin rejuvenation, facial hair removal, body hair removal. **Questions patients commonly ask:** **Is the ZYE device suitable for all skin types?** Yes. The dual‑wavelength system and integrated cooling allow treatment across all Fitzpatrick skin types. **How long does a typical treatment session take?** Treatment time varies by area. Smaller zones may take 10–20 minutes, while larger body areas may require 30–45 minutes, also it depend on the used handpiece **How long do results last?** Hair removal results are long‑term with periodic maintenance. Rejuvenation and pigmentation outcomes develop over several weeks and are maintained with scheduled follow‑up treatments. **Who is ZYE suitable for and what does it treat?** ZYE is suitable for all skin types (Fitzpatrick I-VI) and treats unwanted hair on face and body. Its multi-wavelength technology ensures safe, effective results across diverse skin tones. **What results can I expect from ZYE and is there downtime?** Noticeable hair reduction appears after 2-3 sessions, with 80-90% reduction after a full course of 6-8 sessions. There is no downtime — patients return to normal activities immediately. **Is ZYE safe and what are the side effects?** ZYE is clinically proven safe with integrated skin cooling and contact sensors for protection. Temporary redness or mild warmth in treated areas is common and resolves within hours. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### ZYE **URL:** https://dubaimed.com/products/zye **Brand:** VYDENCE **Product type:** medical_device **Category:** medical-devices **Technical overview:** ZYE is an advanced aesthetic device developed by Vydence Medical, a Brazilian medical technology company specializing in energy-based aesthetic platforms. ZYE is designed as a high-performance diode laser system optimized for hair removal and skin treatments, offering fast treatment speeds and effective results across a range of skin types. The system utilizes diode laser technology at wavelengths specifically selected for optimal absorption by melanin in hair follicles, enabling permanent hair reduction through selective photothermolysis. ZYE features a high-power laser engine capable of delivering rapid pulse repetition rates, allowing practitioners to treat large body areas efficiently within shorter session times. Clinical applications include permanent hair reduction on the face, underarms, bikini line, legs, arms, back, and chest, as well as treatment of pseudofolliculitis barbae (ingrown hairs) and skin rejuvenation. The device is engineered for high patient throughput in busy aesthetic clinics, combining speed with built-in safety features including integrated contact cooling to protect the epidermis during treatment and real-time skin temperature monitoring. **Unique features:** ZYE delivers high-power diode laser energy with rapid pulse repetition rates, enabling practitioners to perform hair removal treatments significantly faster than conventional diode systems. The device features an integrated contact cooling system that maintains epidermal temperature at safe levels throughout treatment, ensuring patient comfort without the need for external cooling devices or topical anesthetics in most cases. ZYE's large spot size applicator covers more skin surface per pulse, reducing overall treatment time for large body areas such as the back and legs. The system supports multiple treatment modes including single-pulse high-fluence mode for coarse hair and in-motion low-fluence repetitive mode for faster coverage of larger areas and treatment of finer hair. Built-in skin type detection and energy recommendation algorithms help practitioners select optimal parameters for different Fitzpatrick skin types, enhancing safety across diverse patient populations. The robust, clinic-grade construction is designed for high daily patient volumes with minimal maintenance requirements. **Clinical indications:** - aesthetic treatment - clinic technology - hair removal - permanent hair reduction - pseudofolliculitis barbae - ingrown hairs - skin rejuvenation - facial hair removal - body hair removal **Clinician FAQs:** **Is the ZYE device suitable for all skin types?** Yes. The dual‑wavelength system and integrated cooling allow treatment across all Fitzpatrick skin types. **Does the ZYE device cause discomfort during treatment?** Most patients feel mild warmth or brief stinging depending on wavelength and fluence. COOL‑&‑CLEAR® cooling helps manage surface heat. **How long do results last?** Hair removal results are long‑term with periodic maintenance. Rejuvenation and pigmentation outcomes develop over several weeks and are maintained with scheduled follow‑up treatments. **Does the ZYE device require any special maintenance?** Routine system checks and handpiece calibration are recommended. WiFi connectivity supports remote monitoring and technical oversight. **What is ZYE and how does it work?** ZYE is a high-performance diode laser by VYDENCE featuring multiple wavelengths for effective hair removal and skin treatments, delivering energy precisely to target follicles and chromophores. **Who is ZYE suitable for and what does it treat?** ZYE is suitable for all skin types (Fitzpatrick I-VI) and treats unwanted hair on face and body. Its multi-wavelength technology ensures safe, effective results across diverse skin tones. **What does a ZYE laser treatment session involve?** The area is shaved and a cooling gel may be applied. The ZYE handpiece glides over the skin delivering rapid laser pulses. Built-in cooling ensures comfort. Sessions take 15-60 minutes by area. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### ZYE **Brand:** VYDENCE **Type:** medical_device **Portfolio status:** direct portfolio SmartLASER platform for skin rejuvenation and hair removal **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: Ellacor **Canonical URL:** https://dubaimed.com/products/ellacor **Brand:** CYTRELLIS ### For patients ### Ellacor **Learn more:** https://dubaimed.com/products/ellacor Non‑surgical FDA Cleared Micro-Coring™ Technology **What it treats:** moderate wrinkles, severe wrinkles, facial wrinkles, mid face wrinkles, lower face wrinkles, skin laxity, sagging skin, excess skin, jowls, marionette lines, nasolabial folds, perioral wrinkles, jawline laxity, skin tightening, fractional skin resurfacing, body skin laxity, abdomen laxity, arm laxity, knee laxity. **Regulatory status:** FDA-cleared. **Questions patients commonly ask:** **How does Ellacor work?** Hollow needles remove micro‑cores of skin in a controlled pattern. The body closes these openings through natural healing, leading to visible improvement in wrinkles. **Does the procedure use heat?** No. Ellacor does not use or generate heat, reducing the risk of thermal injury. **Is there downtime?** Downtime varies by patient, but most experience temporary redness, swelling, or mild bruising. Recovery is generally shorter than surgical alternatives. **How many treatments are needed?** Treatment plans vary. Some patients see improvement after one session, while others may require additional procedures based on clinical goals. **Is ellacor suitable for all skin types** Suitability is determined by the practitioner. The device is cleared for wrinkle reduction in the mid and lower face, and patient selection is based on clinical evaluation. **Who is Ellacor suitable for?** Ellacor is indicated for adult patients with moderate-to-severe cheek wrinkles. The non-thermal mechanism makes it a strong option across multiple skin types, though current FDA clearance is primarily on Fitzpatrick I-IV. Clinical evaluation for darker phototypes is ongoing. **How is Ellacor different from fractional lasers and microneedling RF?** Ellacor is non-thermal, which avoids the PIH and pigmentation risks seen with fractional laser and RF microneedling in darker skin types. It physically removes skin rather than heating it, producing net tissue reduction rather than coagulation. **What conditions does Ellacor treat and who is the ideal patient?** Ellacor is FDA-cleared for moderate to severe wrinkles in the mid and lower face (adults 22+, Fitzpatrick I-IV). In November 2025, it received a second FDA clearance for Fractional Skin Resurfacing, expanding use to any body area with skin laxity — abdomen, knees, arms, and more. Specific facial concerns include nasolabial folds, marionette lines, perioral wrinkles, jawline laxity, jowls, and lower cheek wrinkles. The ideal patient is typically aged 40-60, just beginning to develop jowls and facial lines, but not ready for surgery or unwilling to undergo a surgical facelift. It's also suitable for patients who've had a facelift and want maintenance without a second surgery. **What does an Ellacor treatment session involve?** The procedure takes approximately 30 minutes. First, topical numbing cream is applied, followed by local anesthetic injections (lidocaine with epinephrine). For the perioral area, nerve blocks are performed for additional comfort — most patients report pain as less than 2 on a 0-10 scale during the procedure. The practitioner selects skin removal density (1-8%) and core depth (0-4mm) based on the anatomical area, then moves the handpiece across the treatment zone. The device uses a footswitch, and the integrated vacuum stabilizes the skin during coring. After treatment, the face is wiped with chilled sterile water and a thin film of petrolatum is applied. The recommended protocol is 2-3 sessions spaced 30 days apart, with follow-up visits at 48-72 hours, 30 days, and 60 days. **What results can I expect and how much downtime is there?** In the pivotal clinical trial, 90% of patients showed improvement in moderate to severe wrinkles on the Global Aesthetic Improvement Scale, and 86% reported overall satisfaction. Results begin developing as healing progresses — visible wrinkle reduction is typically appreciated at approximately 6 weeks, with full results at around 3 months as collagen remodels. Downtime is moderate: 70% of patients were comfortable going out in public or returning to work 3 days post-procedure. The typical downtime period is 7-10 days, during which redness, swelling, bruising, and skin tightness are common. After the initial downtime, residual redness may remain but can be concealed with makeup. Higher density settings produce more dramatic results but with proportionally longer downtime. **Is Ellacor safe? What are the side effects and contraindications?** Ellacor has been evaluated in over 200 patients across clinical sites with safety confirmed at densities up to 10% and depths up to 4mm with complete epithelialization. Common side effects include redness, swelling, bruising, skin tightness, dryness, peeling, crusting, tenderness, bleeding, numbness, tingling, and circular marks — most resolving within days to two weeks. At 30 days, redness was present in less than 20% of patients. Uncommon side effects may include hyper/hypopigmentation, hematoma, infection, skin irregularities, or scarring. Contraindications: pregnancy/nursing, history of keloids, bleeding disorders, allergy to anesthesia or stainless steel, autoimmune conditions, active skin cancer, open wounds, facial implants in treatment area. Patients must stop anticoagulants/NSAIDs 14 days before and cannot have had cosmetic injections/fillers in the area for 6 months prior. Currently indicated for Fitzpatrick I-IV only. **What post-treatment care is required after an Ellacor procedure?** Post-procedure care is straightforward but important for optimal healing. Apply a lanolin-free healing ointment (CeraVe or Cetaphil recommended) twice daily. Apply a thin film of petrolatum at least twice daily for seven days. Avoid sunscreen and makeup for 3-4 days to prevent product buildup within the micro-cores. Cleanse the treated area twice daily with water and a mild facial cleanser — do not scrub or rub vigorously. After the skin has fully healed (no open wounds, cores closed), apply sunscreen and limit sun exposure for at least 2 weeks (longer if erythema persists, as sun exposure can cause hyperpigmentation). Avoid: shaving, tanning beds, scratching or picking the treated area, submerging in pools/oceans, and activities causing overheating (hot baths, excessive exercise) until fully healed. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Ellacor **URL:** https://dubaimed.com/products/ellacor **Brand:** CYTRELLIS **Product type:** medical_device **Category:** medical-devices **Technical overview:** Ellacor is the first and only FDA-cleared procedure to non-surgically remove excess skin — a paradigm-shifting device that uses patented Micro-Coring Technology to physically extract tiny columns of skin tissue, allowing the surrounding skin to naturally contract and heal with no evidence of scarring. Manufactured by Cytrellis Biosystems (Woburn, MA), co-founded by Dr. Rox Anderson and Dr. Jay Austen in partnership with Massachusetts General Hospital. DUBIMED is the authorized distributor in the UAE and GCC region. HOW IT WORKS: Ellacor uses specially designed hollow coring needles that penetrate the skin and excise full-thickness micro-cores of epidermal and dermal tissue. The internal diameter of each needle is less than 0.5mm — below the threshold that may cause scarring (Champlain et al., 2019). An integrated vacuum system stabilizes the skin during tissue removal, and the excised cores are evacuated by suction. After removal, micro-cores close rapidly along the relaxed skin tension lines (confirmed by OCT imaging at approximately 10 minutes post-procedure). The body's natural healing response then contracts the surrounding skin, resulting in tighter, smoother skin with visibly reduced wrinkles. Unlike RF microneedling, ablative lasers, or ultrasound devices, Ellacor removes skin cleanly without thermal energy. Ablative lasers leave behind Microepidermal Necrotic Debris (MENDs) that prevent early closure of micro-cores and limit skin surface area reduction. Ellacor's non-thermal approach eliminates this problem entirely. DEVICE SPECIFICATIONS: - Skin Removal Percentage: 1%, 3%, 5%, 7%, 8% (higher = more aggressive treatment) - Treatment Window: 10mm x 10mm - Core Depth: 0.0–4.0mm, adjustable in 0.5mm increments - Maximum Core Count: 24,000 cores per single-use cartridge - Integrated vacuum system for skin stabilization and tissue evacuation - Touchscreen with intuitive interface - Lightweight, ergonomic handpiece with footswitch operation RECOMMENDED DEPTH/DENSITY BY AREA (Clinical Pearls, Dr. H. Ray Jalian): - Upper Lip: 2mm depth, 5-7% density - Chin: 2.5mm, 3-5% - Medial Jawline: 2.5-3mm, 5-7% - Lateral Jawline: 3-4mm, 5-7% - Medial Cheek (buccal): 4mm, 5-7% - Lateral Cheek (zygoma): 3-4mm, 5-7% FDA CLEARANCES: 1. Original clearance: Treatment of moderate and severe wrinkles in the mid and lower face in adults aged 22+ with Fitzpatrick skin types I-IV 2. November 2025 — 510(k) K252752: Fractional Skin Resurfacing — expands use to any body area where skin laxity is a concern (abdomen, knees, arms, etc.) PIVOTAL CLINICAL STUDY (ClinicalTrials.gov NCT 03573271): - 51 subjects completed the study; treated 2-3 times with 7-8% skin removal and up to 5mm coring depth - 90% of patients showed improvement on the Global Aesthetic Improvement Scale (GAIS) - 86% overall patient satisfaction - Evaluated in 200+ patients across clinical sites - Pain reported as less than 2 on 0-10 Wong-Baker Scale - Safety confirmed at densities up to 10% and depths up to 4mm with complete epithelialization - No evidence of scarring TREATMENT PROTOCOL: - Procedure duration: approximately 30 minutes - Recommended: 2-3 sessions spaced 30 days apart - Anesthesia: topical numbing + local infiltration (lidocaine 1-2% with epinephrine); nerve blocks for perioral area - Post-procedure: healing ointment (CeraVe/Cetaphil, lanolin-free) twice daily; petrolatum film for 7 days; no sunscreen/makeup for 3-4 days; limit sun exposure 2+ weeks - Downtime: 70% of patients comfortable going out in public at 3 days; typical downtime 7-10 days; full results at approximately 3 months; visible wrinkle reduction at 6 weeks - Follow-up visits: 48-72 hours, 30 days, 60 days post-procedure CONTRAINDICATIONS: Pregnancy/nursing, history of keloids, bleeding disorders, allergy to anesthesia or stainless steel, autoimmune conditions, active skin cancer, open wounds/sores, facial implants in treatment area. No high-dose anticoagulants/NSAIDs for 14 days pre-treatment. No cosmetic injections/fillers in treatment area for 6 months prior. No facial surgery within 12 months. Currently indicated for Fitzpatrick I-IV only (separate study needed for V-VI). IDEAL PATIENT PROFILE: Patients aged 40s-60s with beginning jowls, marionette lines, perioral lines, fine lines in lower cheeks — not ready for surgery or unwilling to undergo surgery. Also suitable for patients who have had a facelift and want maintenance without a second surgery. AWARDS & MEDIA: NewBeauty 2023 Award Winner. Featured in ELLE, Allure, Harper's Bazaar, Men's Health, Forbes, Wall Street Journal, InStyle, RealSelf, Modern Aesthetics, MedEsthetics, Dermatology Times, POPSUGAR, Town & Country, Healio, AEDIT, Byrdie. Over 4 billion media impressions. **Unique features:** 1. FIRST AND ONLY NON-SURGICAL SKIN REMOVAL DEVICE: Ellacor is the only FDA-cleared device that physically removes excess skin without surgery. While lasers, RF, and ultrasound devices induce thermal injury to trigger remodeling, Ellacor actually excises and removes skin tissue — a fundamentally different mechanism that produces true skin contraction, not just collagen tightening. 2. PATENTED MICRO-CORING TECHNOLOGY — NO THERMAL ENERGY: Hollow coring needles (<0.5mm internal diameter) extract full-thickness micro-cores of epidermal and dermal tissue without any heat, laser, radiofrequency, or ultrasound energy. This eliminates thermal injury risks (burns, prolonged erythema, PIH) and avoids Microepidermal Necrotic Debris (MENDs) that ablative lasers leave behind, allowing faster core closure and actual skin surface area reduction. 3. CO-FOUNDED BY PIONEERS — DR. ROX ANDERSON & DR. JAY AUSTEN: Co-founded by Dr. Rox Anderson (inventor of selective photothermolysis, fractional photothermolysis, and CoolSculpting) and Dr. Jay Austen, in partnership with Massachusetts General Hospital. This pedigree in aesthetic device innovation is unmatched. 4. DUAL FDA CLEARANCES — FACE + FULL BODY (2025): Original clearance for moderate-to-severe wrinkles in mid/lower face (Fitzpatrick I-IV, aged 22+). In November 2025, received 510(k) K252752 for Fractional Skin Resurfacing — expanding use to any body area with skin laxity (abdomen, knees, arms, etc.). 5. PRECISION-ADJUSTABLE SETTINGS: Skin removal density (1%, 3%, 5%, 7%, 8%) and core depth (0.0-4.0mm in 0.5mm increments) are independently adjustable, allowing practitioners to customize treatment intensity per anatomical area. Treatment window is 10mm x 10mm per stamp. Maximum 24,000 cores per single-use cartridge. 6. INTEGRATED VACUUM SYSTEM: Vacuum stabilizes the skin during coring and evacuates excised tissue through suction tubing, maintaining a clean treatment field. Cores close rapidly along relaxed skin tension lines — OCT imaging confirms hole absence within approximately 10 minutes post-procedure. 7. CLINICALLY PROVEN — 90% IMPROVEMENT, 86% SATISFACTION: Pivotal study (NCT 03573271): 90% showed improvement on GAIS, 86% overall satisfaction. 200+ patients evaluated across clinical sites. Pain rated <2 on 0-10 scale. Safety confirmed at densities up to 10% and depths up to 4mm. Published in PRS Global Open (Pozner et al., 2021). 8. BRIDGES THE GAP BETWEEN ENERGY DEVICES AND SURGERY: Fills a previously empty treatment gap — more effective than energy-based skin rejuvenation (which cannot remove skin) but without the invasiveness, scarring, and extended downtime of a surgical facelift. Ideal for patients aged 40-60 who are not ready for or unwilling to undergo surgery. 9. SCARLESS HEALING BELOW 0.5mm THRESHOLD: Each micro-core is below the scientifically established scarring threshold of 0.5mm diameter (Champlain et al., 2019, Lasers in Surgery and Medicine). This foundational research ensures the technology is inherently scar-free by design, not just by clinical observation. 10. MINIMAL DOWNTIME — 70% PUBLIC-READY AT DAY 3: In the pivotal trial, 70% of patients were comfortable going out in public or returning to work 3 days after the procedure. Full results develop over approximately 3 months as collagen remodels. Visible wrinkle reduction typically appreciated at 6 weeks. **Clinical indications:** - moderate wrinkles - severe wrinkles - facial wrinkles - mid face wrinkles - lower face wrinkles - skin laxity - sagging skin - excess skin - jowls - marionette lines - nasolabial folds - perioral wrinkles - jawline laxity - skin tightening - fractional skin resurfacing - body skin laxity - abdomen laxity - arm laxity - knee laxity **Regulatory status:** - FDA-cleared **Positioning:** Compared against: facelift, surgical facelift, ablative laser, fractional CO2, RF microneedling, ultrasound lifting, thread lift. **Clinician FAQs:** **Is there downtime?** Downtime varies by patient, but most experience temporary redness, swelling, or mild bruising. Recovery is generally shorter than surgical alternatives. **How many treatments are needed?** Treatment plans vary. Some patients see improvement after one session, while others may require additional procedures based on clinical goals. **Is ellacor suitable for all skin types** Suitability is determined by the practitioner. The device is cleared for wrinkle reduction in the mid and lower face, and patient selection is based on clinical evaluation. **What is Ellacor and how does it work?** Ellacor is the first and only FDA-cleared micro-coring device. It removes micro-cores of skin (approximately 500 microns in diameter) without thermal energy, triggering natural skin retraction to reduce moderate-to-severe wrinkles, particularly in the mid and lower face. **Who is Ellacor suitable for?** Ellacor is indicated for adult patients with moderate-to-severe cheek wrinkles. The non-thermal mechanism makes it a strong option across multiple skin types, though current FDA clearance is primarily on Fitzpatrick I-IV. Clinical evaluation for darker phototypes is ongoing. **Is Ellacor available in the UAE?** Yes. DUBIMED distributes Ellacor across the UAE and GCC with training certification from Cytrellis included. Clinics are provided with the full consumable supply chain and biomedical service coverage. **How is Ellacor different from fractional lasers and microneedling RF?** Ellacor is non-thermal, which avoids the PIH and pigmentation risks seen with fractional laser and RF microneedling in darker skin types. It physically removes skin rather than heating it, producing net tissue reduction rather than coagulation. **What conditions does Ellacor treat and who is the ideal patient?** Ellacor is FDA-cleared for moderate to severe wrinkles in the mid and lower face (adults 22+, Fitzpatrick I-IV). In November 2025, it received a second FDA clearance for Fractional Skin Resurfacing, expanding use to any body area with skin laxity — abdomen, knees, arms, and more. Specific facial concerns include nasolabial folds, marionette lines, perioral wrinkles, jawline laxity, jowls, and lower cheek wrinkles. The ideal patient is typically aged 40-60, just beginning to develop jowls and facial lines, but not ready for surgery or unwilling to undergo a surgical facelift. It's also suitable for patients who've had a facelift and want maintenance without a second surgery. **How is Ellacor different from microneedling, lasers, and RF devices?** Ellacor is fundamentally different from all energy-based devices. Microneedling uses small needles to injure tissue, but the tissue is only temporarily displaced — not removed. Lasers and RF devices use heat to induce thermal injury and collagen remodeling. Ellacor is the first device to actually remove skin on the micro-scale. This distinction matters clinically: ablative lasers leave behind Microepidermal Necrotic Debris (MENDs) that prevent early closure and limit skin surface area reduction. Ellacor cleanly removes tissue, allowing rapid core closure and actual skin contraction. As Dr. Steven Cohen puts it: "Its Micro-Coring treatment fits somewhere between energy-based skin rejuvenation and actual face-lift surgery." **What does an Ellacor treatment session involve?** The procedure takes approximately 30 minutes. First, topical numbing cream is applied, followed by local anesthetic injections (lidocaine with epinephrine). For the perioral area, nerve blocks are performed for additional comfort — most patients report pain as less than 2 on a 0-10 scale during the procedure. The practitioner selects skin removal density (1-8%) and core depth (0-4mm) based on the anatomical area, then moves the handpiece across the treatment zone. The device uses a footswitch, and the integrated vacuum stabilizes the skin during coring. After treatment, the face is wiped with chilled sterile water and a thin film of petrolatum is applied. The recommended protocol is 2-3 sessions spaced 30 days apart, with follow-up visits at 48-72 hours, 30 days, and 60 days. **What results can I expect and how much downtime is there?** In the pivotal clinical trial, 90% of patients showed improvement in moderate to severe wrinkles on the Global Aesthetic Improvement Scale, and 86% reported overall satisfaction. Results begin developing as healing progresses — visible wrinkle reduction is typically appreciated at approximately 6 weeks, with full results at around 3 months as collagen remodels. Downtime is moderate: 70% of patients were comfortable going out in public or returning to work 3 days post-procedure. The typical downtime period is 7-10 days, during which redness, swelling, bruising, and skin tightness are common. After the initial downtime, residual redness may remain but can be concealed with makeup. Higher density settings produce more dramatic results but with proportionally longer downtime. **Is Ellacor safe? What are the side effects and contraindications?** Ellacor has been evaluated in over 200 patients across clinical sites with safety confirmed at densities up to 10% and depths up to 4mm with complete epithelialization. Common side effects include redness, swelling, bruising, skin tightness, dryness, peeling, crusting, tenderness, bleeding, numbness, tingling, and circular marks — most resolving within days to two weeks. At 30 days, redness was present in less than 20% of patients. Uncommon side effects may include hyper/hypopigmentation, hematoma, infection, skin irregularities, or scarring. Contraindications: pregnancy/nursing, history of keloids, bleeding disorders, allergy to anesthesia or stainless steel, autoimmune conditions, active skin cancer, open wounds, facial implants in treatment area. Patients must stop anticoagulants/NSAIDs 14 days before and cannot have had cosmetic injections/fillers in the area for 6 months prior. Currently indicated for Fitzpatrick I-IV only. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Ellacor **Brand:** CYTRELLIS **Type:** medical_device **Portfolio status:** direct portfolio Non‑surgical FDA Cleared Micro-Coring™ Technology **Market access:** FDA-cleared. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **Is Ellacor available in the UAE?** Yes. DUBIMED distributes Ellacor across the UAE and GCC with training certification from Cytrellis included. Clinics are provided with the full consumable supply chain and biomedical service coverage. ## Product: AnteAGE® MDX Biosome™ **Canonical URL:** https://dubaimed.com/products/anteage-mdx-biosome **Brand:** AnteAGE ### For patients ### AnteAGE® MDX Biosome™ **Learn more:** https://dubaimed.com/products/anteage-mdx-biosome Biomimetic exosome technology **What it treats:** anti-aging, skin rejuvenation, collagen stimulation, elastin production, pore reduction, skin tightening, hyperpigmentation, melasma, age spots, sun damage, uneven skin tone, hair loss, androgenic alopecia, wound healing, post-procedure recovery. **Questions patients commonly ask:** **What is ANTEAGE MDX BIOSOME™?** ANTEAGE MDX BIOSOME™ is an advanced regenerative skincare platform that uses synthetic Biosomes™ to mimic the beneficial effects of natural exosomes. These lipid nanoparticles deliver targeted regenerative signals to the skin, supporting collagen production, repair, and overall rejuvenation. **How do Biosomes™ work?** Biosomes™ act as controlled bio-signal carriers, entering skin cells and delivering growth factors and proteins that trigger repair and regeneration pathways. Their optimised lipid shell and nanoscale size allow efficient penetration and intracellular delivery, supporting improvements in firmness, elasticity, and texture. **Is it suitable for all skin types?** Yes, Biosomes™ are designed to be safe and effective across all skin types, with controlled composition that reduces the variability seen in some biologic preparations. Practitioners still assess individual history, sensitivities, and concurrent treatments to tailor protocols and optimise comfort and results. **What is AnteAGE MDX Biosome?** AnteAGE MDX Biosome is a topical post-procedure serum delivering bone-marrow-derived MSC growth factors and cytokines encapsulated in biosomes for enhanced delivery into freshly treated skin. Developed specifically for use after microneedling, fractional laser, and RF treatments. **What does each AnteAGE MDX Biosome product treat?** 1. BIOSOME SOLUTION (Skin) — 5×3mL: GF payload: TGFb3, HGF, KGF-1/2, NGF, SIRT-1/2, TRX, TIMP-1, hBD3H via HMW HA carrier. Best for: Acne scars | Enlarged pores | Fine lines & wrinkles | Skin tightening | Collagen & elastin rebuilding | Post-treatment recovery | Skin vitality. 2. BIOSOME BRIGHTENING SOLUTION — 5×3mL: Attacks 8 pigmentation pathways simultaneously. Key actives: - 8.5% Tranexamic Acid: disrupts melanocyte-keratinocyte signaling + inhibits tyrosinase → reduces melanin production - Acetyl Glucosamine: reduces melanogenesis, synergistic with Niacinamide - HMW HA: lubrication + rehydration for microneedling - Peptides: Tetrapeptide-30, Nonapeptide-1, sh-Oligopeptide-33, sh-Polypeptide-58 Best for: Melasma | Hyperpigmentation | Dark spots | PIH (post-inflammatory hyperpigmentation) | Sun damage | Uneven skin tone. No drying, irritation, or inflammation. 3. BIOSOME HAIR SOLUTION — 3×5mL: - WNT-Specific Biosomes: activate WNT signaling (master regulator of follicle stem cells) via direct cellular entry - Shikimic Acid: prolongs anagen (active growth) phase — 2019 Korean clinical study - Azelaic Acid: blocks 5α-reductase → reduces DHT (root cause of androgenic alopecia) - Caffeine: scalp vasodilation + blood flow Best for: Androgenic alopecia | Hair thinning | Hair density | Scalp health | Post-hair transplant. **How is AnteAGE MDX Biosome applied in clinical treatments?** Biosome products are for professional in-clinic use, applied during or immediately after skin procedures: Best treatment combinations: - Microneedling (dermal): Apply Biosome Solution as the microneedling serum — micro-channels dramatically increase penetration into the dermis. - RF Microneedling (Secret DUO, Morpheus8): Apply immediately post-procedure for enhanced recovery and regeneration. - Laser (CO2, fractional, Er:YAG): Post-laser to reduce inflammation, accelerate healing, amplify collagen remodeling. - Energy-based (IPL, RF, ultrasound): Post-treatment to calm skin and initiate regeneration. - Standalone: Apply with nano-needling or electroporation as a primary rejuvenation treatment. Application: Each set = lyophilized Biosome vial + HMW HA diluent vial. Add diluent to lyophilized powder. Mix gently. Apply to treatment area immediately. For Brightening and Hair: same process with respective diluents. **Is AnteAGE MDX Biosome safe? What are its certifications?** AnteAGE MDX Biosome has an excellent safety profile: Safety certifications: - NAMSA OECD 471 Cell Safe Testing: Independent genotoxicity testing by NAMSA — one of the world's leading medical device testing organizations. - FDA MoCRA #53-603116-583651: Fully registered July 2024 under the Modernization of Cosmetic Regulation Act. - GMP Certified manufacturing | ISO 7 Clean Room Clinical safety: - Non-human derived: No human cells, no donor biological material — zero pathogen transmission or immune reaction risk. - Non-immunogenic: No immune response. - Zero allergens. - Suitable for all skin types and all Fitzpatrick skin types. - No reported adverse reactions in clinical use. - No drying, irritation, or inflammation (Brightening formula specifically designed for this). **How does Biosome Brightening target pigmentation?** Biosome Brightening attacks 8 pigmentation pathways simultaneously — making it the most comprehensive professional brightening treatment available. 1. Tranexamic Acid (8.5%) — multi-pathway action: - Reduces melanocyte-keratinocyte communication → disrupts the signal that triggers melanin production - Inhibits tyrosinase enzyme → directly reduces melanin synthesis - Anti-fibrinolytic: prevents plasmin-mediated arachidonic acid release that stimulates melanocyte activity 2. Acetyl Glucosamine: - Highly bioavailable, stable glucosamine form - Clinically proven to reduce melanogenesis - Synergistic with Niacinamide - Inhibits glycosylation of pro-tyrosinase → prevents tyrosinase activation 3. 25 Billion Biosomes: - Provide regenerative scaffold: TGF-b3, KGF, NGF stimulate healthy cell renewal - Replace pigmented cells with new healthy keratinocytes faster 4. HMW Hyaluronic Acid: - Microneedling lubrication and slip during application - Rapid rehydration and volume enhancement in upper skin layers No drying. No irritation. No inflammation. Safe for all skin types. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### AnteAGE® MDX Biosome™ **URL:** https://dubaimed.com/products/anteage-mdx-biosome **Brand:** AnteAGE **Product type:** soft-product **Category:** soft-products **Technical overview:** AnteAGE MDX Biosome is the next evolution in regenerative skincare — an FDA MoCRA-registered professional treatment system built on Biomimetic Exosome Technology (BIOSOMES™). Developed by Cellese Biological Lab (USA) and distributed in the Middle East exclusively by DUBIMED. WHAT ARE BIOSOMES? Biosomes are engineered synthetic exosome mimics — lipid nanoparticles (100nm diameter) created through nanomanufacturing. They contain recombinant human proteins designed to replicate the function of natural exosomes. Unlike real exosomes which must be cultured from living stem cells, Biosomes are manufactured with full quality control, making them room temperature stable with longer-lasting activity. Biosomes combine signals from TWO stem cell sources: - Bone Marrow Mesenchymal Exosomes: "Command and control" over healing and inflammation - Umbilical Cord Mesenchymal Exosomes: Highly proliferative regenerative factors This dual-source hybrid is exclusive to AnteAGE MDX Biosome. KEY SPECIFICATIONS: - 25 Billion Pure Biosomes per treatment - 100nm Diameter lipid nanoparticles - ~500% more biological signal concentration vs. GF alone - Room temperature stable — no cold chain required - NAMSA OECD 471 Cell Safe Testing certified - FDA MoCRA #53-603116-583651 (registered July 2024) - Made in USA, ISO 7 Class Clean Room, GMP Certified BIOSOME LIPID BILAYER (structural components): Phosphatidylcholine (cell membrane structure) | Phosphatidylserine (cell turnover, skin renewal) | Sphingomyelin (skin barrier function) | Cholesterol (membrane fluidity, moisture, elasticity) MAIN GROWTH FACTORS: TGFb3 (collagen production) | HGF (tissue regeneration + wound healing) | KGF-1 (keratinocyte proliferation) | KGF-2 (epidermis maintenance) | NGF (skin vitality) | SIRT-1 (cellular repair + longevity) | SIRT-2 (cell metabolism + homeostasis) | TRX (antioxidant) | TIMP-1 (extracellular matrix integrity) | hBD3H (skin defense) THREE PRODUCT LINES: 1. BIOSOME SOLUTION (Skin Anti-Aging) — 5×3mL lyophilized vials + HMW HA diluent: Targets anti-aging, collagen and elastin stimulation, pore reduction, skin tightening. 2. BIOSOME BRIGHTENING SOLUTION — 5×3mL: The only professional brightening product targeting 8 pigmentation pathways simultaneously. - 8.5% Tranexamic Acid: Reduces melanocyte-keratinocyte communication; inhibits tyrosinase enzyme → reduces melanin production directly - Acetyl Glucosamine: Reduces melanogenesis; synergistic with Niacinamide - HMW HA: Microneedling lubrication + rapid rehydration - Peptide complex: Tetrapeptide-30, Nonapeptide-1, sh-Oligopeptide-33, sh-Polypeptide-58 No drying, irritation, or inflammation. 3. BIOSOME HAIR SOLUTION — 3×5mL: WNT-specific Biosomes + Shikimic Acid + Azelaic Acid + Caffeine + HMW HA. - WNT Biosomes: Direct cellular entry activates dormant follicle stem cells (more powerful than topical WNT alone) - Shikimic Acid: 2019 Korean study — significantly prolongs anagen (active growth) phase - Azelaic Acid: Blocks 5α-reductase → reduces DHT production (primary driver of androgenic hair loss) - Caffeine: Increases scalp blood flow; established hair growth stimulator **Unique features:** 1. BIOSOMES™ — THE WORLD'S MOST ADVANCED SYNTHETIC EXOSOME PLATFORM: Biosomes enter neighboring cells without needing a receptor — just like natural exosomes — delivering regenerative signals directly. Invented exclusively by Cellese after 11+ years of stem cell research to capture the full potential of exosomes in a controlled manufacturing process. 2. DUAL-SOURCE HYBRID (BONE MARROW + UMBILICAL CORD): The only product combining Bone Marrow MSC secretome (healing/inflammation control) with Umbilical Cord MSC secretome (proliferative regeneration) in a single formulation. Clinical studies confirm this dual approach produces superior outcomes. 3. ~500% MORE BIOLOGICAL SIGNAL CONCENTRATION VS. GF ALONE: In vitro studies: ~500% more signal concentration vs. standard GF solutions. Scratch assay wound healing studies: 200% increase in wound healing potential vs. control. 100% increase in collagen production (cell studies). 4. ROOM TEMPERATURE STABLE — NO COLD CHAIN: Unlike real exosomes requiring 2°C–8°C refrigeration, Biosomes are engineered for room temperature stability. Eliminates cold chain logistics, simplifies clinic stocking and handling. 5. THREE SPECIALIZED FORMULATIONS: - BIOSOME SOLUTION (Skin): Anti-aging, collagen+elastin, pore reduction, tightening | TGFb3, HGF, KGF-1/2, NGF, SIRT-1/2, TRX, TIMP-1, hBD3H - BIOSOME BRIGHTENING: 8 pigmentation pathways | 8.5% Tranexamic Acid + Acetyl Glucosamine + Peptide complex | No drying or irritation - BIOSOME HAIR: WNT follicle activation + Shikimic Acid anagen prolongation + Azelaic Acid DHT block + Caffeine vasodilation 6. FDA MoCRA #53-603116-583651 — Registered July 2024. 7. NAMSA OECD 471 CELL SAFE CERTIFIED — Independent genotoxicity safety testing. 8. ZERO ALLERGENS — Non-human-derived, non-immunogenic. **Clinical indications:** - anti-aging - skin rejuvenation - collagen stimulation - elastin production - pore reduction - skin tightening - hyperpigmentation - melasma - age spots - sun damage - uneven skin tone - hair loss - androgenic alopecia - wound healing - post-procedure recovery **Clinician FAQs:** **How is ANTEAGE MDX BIOSOME™ different from natural exosomes?** Natural exosomes can vary in composition and performance because they are derived from human cells and influenced by donor and processing variables. In contrast, Biosomes™ are synthetically engineered for precision, giving practitioners a more consistent, controllable, and repeatable tool for skin rejuvenation. **Is ANTEAGE MDX BIOSOME™ safe?** ANTEAGE MDX BIOSOME™ is registered under the FDA Modernization of Cosmetic Regulation Act (MOCRA), supporting compliance with modern cosmetic safety requirements. Its synthetic, well-defined composition and controlled production process are designed to minimise variability and support a favourable safety profile when used as directed **Which concerns can it address?** Biosomes™ are used in protocols for global skin rejuvenation, including fine lines, wrinkles, textural irregularities, enlarged pores, and photo-ageing signs. Dedicated programmes can also be configured to support acne scars, pigmentation concerns, and scalp health goals, as permitted by local guidelines. **Is it suitable for all skin types?** Yes, Biosomes™ are designed to be safe and effective across all skin types, with controlled composition that reduces the variability seen in some biologic preparations. Practitioners still assess individual history, sensitivities, and concurrent treatments to tailor protocols and optimise comfort and results. **Where can patients learn more?** Patients interested in ANTEAGE MDX BIOSOME™ should consult their aesthetic healthcare professional for a personalised assessment and treatment plan. The practitioner can explain how Biosomes™ fit within broader protocols such as microneedling, laser, or chemical procedures and outline expected outcomes over time. **Is AnteAGE MDX Biosome the same as exosomes?** No. AnteAGE MDX Biosome uses bone-marrow MSC-derived signals delivered via proprietary biosomes — a different mechanism to donor-derived exosome products. The regulatory profile is cleaner in markets where exosome regulation is still maturing. **What is the difference between a Biosome and a real Exosome?** Real Exosomes (AnteAGE MDX Exosome): - Genuine extracellular vesicles produced by living Bone Marrow Stem Cells - 6,000+ unique natural growth factors, cytokines, mRNA, and lipids - Must be refrigerated (2°C–8°C) and cold-chained - 5 Billion per treatment Biosomes (AnteAGE MDX Biosome): - Engineered synthetic lipid nanoparticles — manufactured, not cultured - Selected recombinant human proteins loaded into lipid nanoparticles - Room temperature stable — no refrigeration or cold chain needed - Non-human-derived, non-immunogenic - 25 Billion per treatment (5x more particles) - Customized per indication: Skin, Brightening, and Hair each have unique Biosome formulas - FDA MoCRA registered Both achieve equivalent biological activity in vitro. Biosome = stability + customizability + higher particle count. Exosome = maximum biological complexity + 6,000 natural growth factors. **What does each AnteAGE MDX Biosome product treat?** 1. BIOSOME SOLUTION (Skin) — 5×3mL: GF payload: TGFb3, HGF, KGF-1/2, NGF, SIRT-1/2, TRX, TIMP-1, hBD3H via HMW HA carrier. Best for: Acne scars | Enlarged pores | Fine lines & wrinkles | Skin tightening | Collagen & elastin rebuilding | Post-treatment recovery | Skin vitality. 2. BIOSOME BRIGHTENING SOLUTION — 5×3mL: Attacks 8 pigmentation pathways simultaneously. Key actives: - 8.5% Tranexamic Acid: disrupts melanocyte-keratinocyte signaling + inhibits tyrosinase → reduces melanin production - Acetyl Glucosamine: reduces melanogenesis, synergistic with Niacinamide - HMW HA: lubrication + rehydration for microneedling - Peptides: Tetrapeptide-30, Nonapeptide-1, sh-Oligopeptide-33, sh-Polypeptide-58 Best for: Melasma | Hyperpigmentation | Dark spots | PIH (post-inflammatory hyperpigmentation) | Sun damage | Uneven skin tone. No drying, irritation, or inflammation. 3. BIOSOME HAIR SOLUTION — 3×5mL: - WNT-Specific Biosomes: activate WNT signaling (master regulator of follicle stem cells) via direct cellular entry - Shikimic Acid: prolongs anagen (active growth) phase — 2019 Korean clinical study - Azelaic Acid: blocks 5α-reductase → reduces DHT (root cause of androgenic alopecia) - Caffeine: scalp vasodilation + blood flow Best for: Androgenic alopecia | Hair thinning | Hair density | Scalp health | Post-hair transplant. **Is AnteAGE MDX Biosome safe? What are its certifications?** AnteAGE MDX Biosome has an excellent safety profile: Safety certifications: - NAMSA OECD 471 Cell Safe Testing: Independent genotoxicity testing by NAMSA — one of the world's leading medical device testing organizations. - FDA MoCRA #53-603116-583651: Fully registered July 2024 under the Modernization of Cosmetic Regulation Act. - GMP Certified manufacturing | ISO 7 Clean Room Clinical safety: - Non-human derived: No human cells, no donor biological material — zero pathogen transmission or immune reaction risk. - Non-immunogenic: No immune response. - Zero allergens. - Suitable for all skin types and all Fitzpatrick skin types. - No reported adverse reactions in clinical use. - No drying, irritation, or inflammation (Brightening formula specifically designed for this). **What results can I expect from AnteAGE MDX Biosome?** Biosome Solution (Skin Anti-Aging): - Texture and pore improvement: visible from 1 treatment at 2 weeks - Fine line and wrinkle reduction: visible at 1 month - Skin tightening and lifting: visible at 1 month - In vitro: +100% collagen production; +200% wound healing potential Biosome Brightening: - Visible pigmentation reduction: from 1 treatment, apparent at 1 month - Skin tone unification and brightening Biosome Hair: - Initial hair growth improvements: visible from 1 treatment at 2 weeks - Hair density improvement: 2 treatments over 2–3 months - Clinical study (28 participants, 12 weeks): 82% major improvement in hair loss; 50% new hair growth Best protocol: 3 treatments spaced 4–6 weeks apart, combined with in-clinic device treatment (microneedling, RF, laser) for maximum penetration. **How does Biosome Hair Solution treat hair loss?** 1. WNT-Specific Biosomes (Primary Mechanism): WNT signaling is the master pathway controlling hair follicle stem cell activation and the hair growth cycle. WNT growth factors encapsulated in Biosomes enter cells without needing a receptor — directly activating dormant follicle stem cells more powerfully than topical WNT alone. 2. Shikimic Acid: Natural plant metabolite (star anise). 2019 Korean clinical study confirmed it significantly prolongs the anagen (active hair growth) phase — meaning follicles spend more time actively growing hair. 3. Azelaic Acid: Naturally occurring yeast metabolite. Blocks 5α-reductase enzyme → reduces conversion of testosterone to DHT. DHT is the primary driver of androgenic alopecia — reducing it attacks a root cause of hair loss. 4. Caffeine: Vasodilator — increases blood flow to the scalp and follicles, improving nutrient and oxygen delivery. Clinical results: 82% major improvement in hair loss; 50% noticed new hair growth after 1–2 treatments. Results visible within 8–12 weeks. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### AnteAGE® MDX Biosome™ **Brand:** AnteAGE **Type:** soft-product **Portfolio status:** direct portfolio Biomimetic exosome technology **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **How is AnteAGE MDX Biosome stored and shipped?** AnteAGE MDX Biosome requires refrigerated storage (2-8°C). DUBIMED runs a cold-chain distribution pipeline across the UAE and GCC with temperature-logged shipments to every clinic. ## Product: dermamelan® **Canonical URL:** https://dubaimed.com/products/dermamelan **Brand:** MESOESTETIC ### For patients ### dermamelan® **Learn more:** https://dubaimed.com/products/dermamelan Medical depigmentation method for long‑term pigment regulation **What it treats:** melasma, hyperpigmentation, discoloration, sun spots, dark spots, post-inflammatory hyperpigmentation, uneven skin tone, chloasma, age spots. **Questions patients commonly ask:** **How do I know if dermamelan® is suitable for me?** Suitability is determined during a consultation with a medical professional. **Is the treatment painful?** Discomfort varies and is assessed by the practitioner. **Can I continue daily activities?** Most patients resume normal routines with appropriate photoprotection. **When will the results appear?** Visible improvement typically begins within the first few weeks. **What are the advantages over other depigmentation treatments?** dermamelan® targets both visible pigment and the cellular origin of melanin overproduction. **What are the side effects?** Your practitioner will review potential reactions and outline the necessary aftercare requirements. **How does cosmelan compare to other depigmentation treatments like chemical peels or laser?** cosmelan offers a significant advantage over chemical peels and laser treatments because it targets melanin production at the cellular level through tyrosinase inhibition, rather than simply removing superficial pigmented layers. This dual-phase approach — an intensive in-clinic mask followed by a home maintenance cream — delivers more consistent and longer-lasting results with lower risk of post-inflammatory hyperpigmentation (PIH), especially on darker skin tones (Fitzpatrick III–VI). Clinical studies show up to 95% pigmentation reduction. Unlike laser, cosmelan can be used year-round with proper sun protection and is suitable for all skin phototypes. **What is cosmelan?** cosmelan is described as a pioneering depigmentation method developed by mesoestetic for visible pigmentation and the cellular mechanisms responsible for melanin overproduction. **What does cosmelan target?** According to the DUBIMED page, it targets visible pigmentation and the underlying cellular mechanisms behind melanin overproduction. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### dermamelan® **URL:** https://dubaimed.com/products/dermamelan **Brand:** MESOESTETIC **Product type:** soft_product **Category:** soft-products **Technical overview:** cosmelan is mesoestetic's world-leading professional depigmentation method, designed to treat and control skin hyperpigmentation including melasma, sun spots, and post-inflammatory hyperpigmentation. The cosmelan method is a two-phase protocol: Phase 1 involves an in-clinic mask application (cosmelan 1) containing a synergistic blend of azelaic acid, kojic acid, phytic acid, retinol, and ascorbic acid that intensively targets melanin synthesis at multiple levels. Phase 2 is a homecare maintenance regimen (cosmelan 2 cream) applied by the patient over several months to sustain results and prevent recurrence. The treatment works by inhibiting tyrosinase enzyme activity — the key catalyst in melanin production — while simultaneously promoting controlled exfoliation and cellular renewal. cosmelan is clinically proven with over 20 years of use worldwide, suitable for all skin types (Fitzpatrick I-VI) and all phototypes, including darker skin tones often difficult to treat. It is the most widely used professional depigmentation method globally with proven efficacy in reducing pigmentation intensity by up to 95%. The protocol requires professional application and patient compliance with a strict homecare routine and sun protection. **Unique features:** World's #1 professional depigmentation method with over 20 years of clinical use and global presence in 80+ countries. Dual-phase protocol combining intensive in-clinic mask (cosmelan 1) with sustained homecare maintenance (cosmelan 2). Multi-target mechanism inhibiting tyrosinase at multiple levels using azelaic acid, kojic acid, phytic acid, retinol, and ascorbic acid. Clinically proven to reduce pigmentation intensity by up to 95%. Safe for all Fitzpatrick skin types (I-VI) including darker phototypes. Continuous action formula that treats existing pigmentation while preventing new melanin formation. No downtime required — patients resume normal activities after mask removal. **Clinical indications:** - melasma - hyperpigmentation - discoloration - sun spots - dark spots - post-inflammatory hyperpigmentation - uneven skin tone - chloasma - age spots **Positioning:** Also known as: dermamelan. Compared against: depigmenting treatment. **Clinician FAQs:** **Will spots disappear permanently?** Long‑term control is achievable with adherence to the full protocol. **How does cosmelan compare to other depigmentation treatments like chemical peels or laser?** cosmelan offers a significant advantage over chemical peels and laser treatments because it targets melanin production at the cellular level through tyrosinase inhibition, rather than simply removing superficial pigmented layers. This dual-phase approach — an intensive in-clinic mask followed by a home maintenance cream — delivers more consistent and longer-lasting results with lower risk of post-inflammatory hyperpigmentation (PIH), especially on darker skin tones (Fitzpatrick III–VI). Clinical studies show up to 95% pigmentation reduction. Unlike laser, cosmelan can be used year-round with proper sun protection and is suitable for all skin phototypes. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### dermamelan® **Brand:** MESOESTETIC **Type:** soft_product **Portfolio status:** direct portfolio Medical depigmentation method for long‑term pigment regulation **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: SuneKOS **Canonical URL:** https://dubaimed.com/products/sunekos ### For patients ### SuneKOS **Learn more:** https://dubaimed.com/products/sunekos Hyaluronic Acid & Amino Acids for the skin **Questions patients commonly ask:** **What is SuneKOS** SuneKOS contains Hyaluronic Acid & 6 Amino Acids formula: the one and only proven and patented Amino Acids mix to maximally produce collagen and elastin and restore skin elasticity and natural volumes. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### SuneKOS **URL:** https://dubaimed.com/products/sunekos **Category:** soft-products **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### SuneKOS Hyaluronic Acid & Amino Acids for the skin **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: Pento **Canonical URL:** https://dubaimed.com/products/pento **Brand:** CLASSYS ### For patients ### Pento **Learn more:** https://dubaimed.com/products/pento Dual-Wavelength Laser Hair Removal **What it treats:** hair removal, laser hair removal, pigmented lesions, melasma, lentigines, sun spots, cafe-au-lait macules, vascular lesions, telangiectasia, spider veins, tattoo removal, skin rejuvenation, photorejuvenation, pore reduction, skin texture improvement, collagen stimulation, ephelides, freckles. **Regulatory status:** MFDS-approved (Korea). **Questions patients commonly ask:** **What is Pento used for?** Pento is used for skin rejuvenation and the treatment of pigmentation, vascular concerns, acne related marks, and uneven skin tone. **Is Pento treatment safe?** Yes. Pento is designed with advanced safety features and controlled energy delivery to ensure effective treatments with a high safety profile. **Does Pento require downtime?** Pento treatments involve minimal downtime. Most patients can return to normal activities shortly after the session. **Is the treatment painful?** Patients usually experience mild and tolerable sensations during treatment. Comfort is enhanced through built in cooling and customizable settings. **How many sessions are needed to see results?** The number of sessions depends on the skin condition and treatment goals. Many patients notice visible improvement after a few sessions, as recommended by the practitioner. **What is Pento and how does it work?** Pento is a dual-wavelength laser system by CLASSYS that combines Alexandrite (755nm) and Nd:YAG (1064nm) laser technologies in a single platform. It works through selective photothermolysis — laser energy is absorbed by chromophores (melanin, hemoglobin) in target tissue, generating heat that destroys the target while sparing surrounding structures. The 755nm wavelength is optimally absorbed by melanin for treating lighter skin types, while the 1064nm penetrates deeper with less melanin sensitivity for safely treating darker skin types. The system features Real-Time Automatic Adjustment that monitors and corrects output during operation, and GCD gas cooling to protect the skin surface. **What conditions does Pento treat?** Pento treats a wide range of conditions: laser hair removal across all skin types (Fitzpatrick I–VI), pigmented lesions (lentigines, sun spots, cafe-au-lait macules, freckles), melasma, vascular lesions (telangiectasia, spider veins), tattoo removal (multi-color), and skin rejuvenation including photorejuvenation, pore reduction, and texture improvement. The 755nm wavelength is used for melanin-rich targets in lighter skin, while 1064nm is preferred for deeper structures and darker skin types. **What does a Pento treatment session look like?** For hair removal, sessions typically require 6–8 treatments spaced 4–8 weeks apart. The clinician selects the appropriate wavelength based on skin type: 755nm for Fitzpatrick I–III, 1064nm for IV–VI. Larger spot sizes (18–24mm) are used for body areas, smaller (6–12mm) for face. The GCD gas cooling system protects the epidermis. For pigmentation, 1–4 sessions may suffice depending on lesion type and depth. **What results can I expect and is there downtime?** For hair removal, clinical studies show 79–83% improvement across body areas after 5 sessions. For pigmentation, visible lightening typically occurs within 1–3 sessions. Side effects are mild and transitory — temporary redness, slight swelling, and warmth — resolving within hours to days. All adverse reactions in clinical studies resolved within one week with no permanent effects. Downtime is minimal; most patients resume normal activities immediately. **Is Pento safe for dark skin types?** Yes. The 1064nm Nd:YAG wavelength has lower melanin absorption, making it safe and effective for Fitzpatrick skin types IV–VI common in the Middle East and South Asia. Clinical trials confirm transitory side effects only, with no permanent adverse events. The wide pulse width range (up to 300ms) allows longer pulses that are gentler on melanin-rich skin. Pento holds MFDS (Korean FDA) approval No. 20-66. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Pento **URL:** https://dubaimed.com/products/pento **Brand:** CLASSYS **Product type:** medical_device **Category:** medical-devices **Technical overview:** Pento is a dual-wavelength laser surgical system by CLASSYS that combines Alexandrite (755nm) and Nd:YAG (1064nm) laser technologies in a single platform. Listed under CLASSYS's 'Multiple Modality' category, Pento delivers both wavelengths for versatile treatment of hair removal, pigmented lesions, vascular conditions, and skin rejuvenation across all Fitzpatrick skin types (I–VI). The 755nm Alexandrite wavelength offers superior melanin absorption, making it optimal for hair removal and pigmentation treatment in lighter skin types (I–III). The 1064nm Nd:YAG provides deeper tissue penetration with reduced melanin sensitivity, enabling safe treatment of darker skin types (IV–VI) and targeting deeper vascular and pigmented structures. Pento features CLASSYS's proprietary Direct ROD Resonance Technology for alignment-free, precise beam generation, Real-Time Automatic Adjustment that continuously monitors and corrects laser output during operation, Precise GCD (Gas Cooling Device) Technology for epidermal protection, and Square-Wave Pulse Energy delivery that maintains consistent beam quality throughout extended treatment sessions without thermal degradation. The system offers 11 interchangeable spot sizes ranging from 3mm to 24mm across four tip configurations, with pulse widths adjustable from 250 microseconds to 300 milliseconds — one of the widest ranges in its class. Output energy reaches 60–80J with repetition rates of 0.5–10Hz across 11 settings. Pento holds MFDS (Korean FDA) approval No. 20-66 and is classified as a laser surgical device for tissue incision, destruction, and removal. DUBIMED is the authorized distributor for Pento in the UAE and Middle East region. **Unique features:** 1. Dual-Wavelength Platform: Combines 755nm Alexandrite and 1064nm Nd:YAG in one device, covering all skin types (I–VI) without needing separate systems. 2. Direct ROD Resonance Technology: Alignment-free rod design generates precise, powerful beams eliminating calibration drift common in other laser systems. 3. Real-Time Automatic Adjustment: Continuously monitors laser output, wavelength, and focus during operation with instant corrections for consistent treatment delivery. 4. Precise GCD Cooling Technology: Gas-based cooling system protects the epidermal surface during treatment, enhancing patient comfort and safety. 5. Square-Wave Pulse Energy: Delivers consistent beam quality with stable output unaffected by prolonged use — no thermal degradation over long sessions. 6. Industry-Leading Spot Size Range: 11 spot sizes from 3mm to 24mm across four interchangeable tip configurations for precision and speed. 7. Widest Pulse Width Range in Class: 250 microseconds to 300 milliseconds — significantly broader than Candela GentleMax Pro Plus or Cynosure Elite iQ. 8. High Output Energy: 60–80J output with 0.5–10Hz repetition rate across 11 settings for rapid large-area treatments. 9. Blended Wavelength Capability: Clinical evidence supports 70/30 Nd:YAG-to-Alexandrite ratio for optimal results on darker skin with lighter hair. 10. Multi-Application Versatility: Single platform addresses hair removal, pigmentation, vascular lesions, tattoo removal, and skin rejuvenation. **Clinical indications:** - hair removal - laser hair removal - pigmented lesions - melasma - lentigines - sun spots - cafe-au-lait macules - vascular lesions - telangiectasia - spider veins - tattoo removal - skin rejuvenation - photorejuvenation - pore reduction - skin texture improvement - collagen stimulation - ephelides - freckles **Regulatory status:** - MFDS-approved (Korea) **Positioning:** Compared against: Candela GentleMax Pro Plus, Cynosure Elite iQ, Alma Soprano Titanium, Cutera Excel HR, alexandrite laser, nd:yag hair removal. **Clinician FAQs:** **What is Pento and how does it work?** Pento is a dual-wavelength laser system by CLASSYS that combines Alexandrite (755nm) and Nd:YAG (1064nm) laser technologies in a single platform. It works through selective photothermolysis — laser energy is absorbed by chromophores (melanin, hemoglobin) in target tissue, generating heat that destroys the target while sparing surrounding structures. The 755nm wavelength is optimally absorbed by melanin for treating lighter skin types, while the 1064nm penetrates deeper with less melanin sensitivity for safely treating darker skin types. The system features Real-Time Automatic Adjustment that monitors and corrects output during operation, and GCD gas cooling to protect the skin surface. **What conditions does Pento treat?** Pento treats a wide range of conditions: laser hair removal across all skin types (Fitzpatrick I–VI), pigmented lesions (lentigines, sun spots, cafe-au-lait macules, freckles), melasma, vascular lesions (telangiectasia, spider veins), tattoo removal (multi-color), and skin rejuvenation including photorejuvenation, pore reduction, and texture improvement. The 755nm wavelength is used for melanin-rich targets in lighter skin, while 1064nm is preferred for deeper structures and darker skin types. **What makes Pento different from other hair removal lasers like GentleMax Pro or Elite iQ?** Pento offers the widest pulse width range in its class (250 microseconds to 300 milliseconds vs. 2ms minimum on competitors), 11 spot sizes from 3mm to 24mm, CLASSYS's proprietary Square-Wave Pulse Energy for consistent beam quality, Direct ROD Resonance Technology eliminating calibration drift, and Real-Time Automatic Adjustment. It also supports blended dual-wavelength protocols with clinical evidence showing a 70/30 Nd:YAG-to-Alexandrite ratio optimal for darker skin with lighter hair. **What does a Pento treatment session look like?** For hair removal, sessions typically require 6–8 treatments spaced 4–8 weeks apart. The clinician selects the appropriate wavelength based on skin type: 755nm for Fitzpatrick I–III, 1064nm for IV–VI. Larger spot sizes (18–24mm) are used for body areas, smaller (6–12mm) for face. The GCD gas cooling system protects the epidermis. For pigmentation, 1–4 sessions may suffice depending on lesion type and depth. **Is Pento safe for dark skin types?** Yes. The 1064nm Nd:YAG wavelength has lower melanin absorption, making it safe and effective for Fitzpatrick skin types IV–VI common in the Middle East and South Asia. Clinical trials confirm transitory side effects only, with no permanent adverse events. The wide pulse width range (up to 300ms) allows longer pulses that are gentler on melanin-rich skin. Pento holds MFDS (Korean FDA) approval No. 20-66. **What certifications does Pento have?** Pento holds MFDS (Korean FDA) approval No. 20-66, classified as a laser surgical device. CLASSYS distributes to 70+ countries worldwide. DUBIMED is the authorized distributor for the UAE and broader Middle East region. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Pento **Brand:** CLASSYS **Type:** medical_device **Portfolio status:** direct portfolio Dual-Wavelength Laser Hair Removal **Market access:** MFDS-approved (Korea). **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **What certifications does Pento have?** Pento holds MFDS (Korean FDA) approval No. 20-66, classified as a laser surgical device. CLASSYS distributes to 70+ countries worldwide. DUBIMED is the authorized distributor for the UAE and broader Middle East region. ## Product: Sofwave™ **Canonical URL:** https://dubaimed.com/products/sofwave **Brand:** Sofwave Medical ### For patients ### Sofwave™ **Learn more:** https://dubaimed.com/products/sofwave Ultimate Non-Invasive Face Lift & Skin Tightening **What it treats:** fine lines, wrinkle reduction, skin tightening, facial lines, facial rejuvenation, anti-aging, collagen stimulation, elastin stimulation, mid-dermis treatment, face lifting, neck tightening, jowl tightening, brow lifting, nasolabial folds, perioral lines, skin laxity, all skin types, all skin tones, non-surgical facelift. **Regulatory status:** FDA-cleared. **Questions patients commonly ask:** **Is Sofwave™ SUPERB™ safe?** Sofwave™ SUPERB™ incorporates integrated Sofcool™ epidermal cooling to protect the skin surface during treatment. Clinical studies report no serious device‑related adverse events, supporting a favourable safety profile. **Is the treatment painful?** Patients may experience transient warmth or tingling during energy delivery. Sensation varies by individual and can be managed with topical anaesthesia if required. **How many sessions are needed?** Most patients achieve visible improvement after a single session. Additional treatments may be recommended based on clinical assessment. **Is there downtime for Sofwave treatment?** Downtime is minimal. Temporary redness or mild swelling may occur and typically resolves within a short period. **Is Sofwave™ suitable for all skin types?** Yes. Ultrasound energy is not absorbed by melanin, making the treatment appropriate for all Fitzpatrick skin types. **How long does a Sofwave treatment take?** A full-face and neck Sofwave session takes approximately 30-45 minutes. Most patients tolerate the treatment with topical anaesthetic; Sofwave Precise cooling keeps the epidermis comfortable throughout the session. **When do patients see Sofwave results?** Initial tightening is visible within weeks. Full collagen remodelling completes at 3-6 months post-treatment. Clinical studies (Kirkland, Sadick, et al.) report 88-93% global aesthetic improvement scale scores. **What is Sofwave?** Sofwave is an FDA-cleared, non-invasive aesthetic device that treats fine lines and wrinkles using SUPERB™ (Synchronous Ultrasound Parallel Beam) technology. It delivers 7 simultaneous high-frequency ultrasound beams to precisely heat the mid-dermis at 1.5mm depth, stimulating the body's natural collagen and elastin production for tighter, smoother, more youthful-looking skin — with no surgery, no downtime, and no needles. **What areas can Sofwave treat?** Sofwave is primarily designed for facial and neck treatments. It is effective for treating: - Fine lines and wrinkles across the face (forehead, crow's feet, perioral lines, nasolabial folds) - Jaw and jowl tightening - Neck laxity and tightening - Brow lifting - Overall facial skin tightening and rejuvenation Because the energy targets only the mid-dermis at 1.5mm and cannot penetrate deeper than 2mm, it is particularly safe and well-suited for facial areas close to underlying nerves, bones, and blood vessels. **Is Sofwave painful? What does the treatment feel like?** Most patients experience only minimal discomfort during the Sofwave treatment. The sensation is typically described as a mild warmth or brief heat feeling beneath the skin surface as each pulse is delivered. The integrated Sofcool™ active cooling system continuously monitors skin temperature and cools the surface in real time, significantly reducing discomfort compared to non-cooled ultrasound devices. No anesthesia or numbing cream is typically required, making it a very well-tolerated procedure. **Is there any downtime after a Sofwave treatment?** No. Sofwave is a zero-downtime procedure. Patients can return to their normal daily activities immediately after treatment — there are no wounds, no bandages, and no recovery period required. Immediately following the session, some patients may notice slight pinkness or minimal swelling in the treated area, but this typically resolves within a few hours. You can go back to work, exercise, and daily routines the same day. **When will I see results from Sofwave, and how long do they last?** The collagen and elastin regeneration process stimulated by Sofwave takes time to develop. Most patients see gradual improvements over the 12 weeks following treatment, with optimal results typically visible at the 3-month mark. In clinical trials, some patients noticed early improvement as soon as 2 weeks after their first session. Results are long-lasting — typically 12–18 months — as the body continues to remodel newly produced collagen. Maintenance treatments once every 12–18 months are recommended to sustain results. **How long does a Sofwave treatment session take?** A full-face Sofwave treatment takes approximately 30–45 minutes. The procedure requires minimal preparation time, and there is no recovery time needed afterward. This fast treatment time is one of Sofwave's key advantages — it easily fits into a patient's lunch break or busy schedule. The straightforward treatment protocol and intuitive interface also mean that once trained, clinic staff can efficiently administer sessions without delays. **Is Sofwave safe? What are the side effects?** Yes. Sofwave is FDA cleared and has a very strong safety profile validated through clinical trials. No serious adverse events were reported in clinical studies. Because the energy targets only the mid-dermis and cannot penetrate beyond 2mm, there is guaranteed protection of the epidermis, underlying nerves, bones, blood vessels, and facial fat. The Sofcool™ integrated cooling mechanism provides an additional layer of real-time epidermal protection. The most common post-treatment observation is mild, transient redness or minimal swelling that resolves within a few hours. **Who is a good candidate for Sofwave?** Sofwave is suitable for adults aged 22 and above who want to address early to moderate signs of aging — specifically fine lines, wrinkles, and mild-to-moderate skin laxity — without surgery. It is ideal for patients who: - Have fine lines, facial wrinkles, or sagging skin - Want a non-invasive, no-downtime treatment - Have any skin type or skin tone (all Fitzpatrick types) - Prefer a fast, single-session improvement - Are not candidates for or wish to avoid surgical procedures - Are looking for collagen stimulation and long-term skin rejuvenation It is not recommended for pregnant patients or those with active skin infections, pacemakers, or metal implants in the treatment area. **Does Sofwave work for darker skin tones?** Yes — Sofwave is uniquely suitable for all skin types including darker Fitzpatrick IV–VI skin tones. This is because ultrasound energy absorption is determined by the mechanical properties of tissue, not by skin color or melanin content. Unlike laser or IPL-based devices, which carry a significant risk of post-inflammatory hyperpigmentation (PIH) or burns in darker skin, Sofwave poses no such risk. This makes it one of the very few non-invasive skin tightening technologies that can be confidently and safely used across all ethnicities and skin tones. **What makes Sofwave a good business investment for clinics?** Sofwave offers a compelling business case for aesthetic clinics: 1. No ongoing consumables — the solid-state handpiece requires no cartridge replacements, keeping cost of ownership very low 2. Fast ROI — high patient throughput with 30–45 minute sessions and minimal prep time 3. Delegatable treatment — trained clinic staff (not only physicians) can administer treatments, freeing physician time for higher-value procedures 4. Broad patient base — suitable for all skin types, ages 22+, meaning no patient exclusions based on skin tone 5. Single treatment protocol — many patients achieve results in 1–2 sessions, reducing chair time and increasing patient turnover 6. Proven efficacy — 72% patient satisfaction in clinical trials with a strong safety record supports strong word-of-mouth and patient retention 7. FDA cleared — a strong regulatory credential that supports marketing and patient confidence **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Sofwave™ **URL:** https://dubaimed.com/products/sofwave **Brand:** Sofwave Medical **Product type:** medical_device **Category:** medical-devices **Technical overview:** Sofwave is an FDA-cleared, non-invasive aesthetic device that delivers a breakthrough approach to skin tightening and the reduction of fine lines and wrinkles. Developed by Sofwave Medical — founded by pioneers of the global aesthetic industry — Sofwave utilizes proprietary SUPERB™ (Synchronous Ultrasound Parallel Beam) technology to precisely target the mid-dermis at 1.5mm depth, stimulating collagen and elastin regeneration without any damage to the epidermis or the underlying structures. Unlike aggressive energy-based treatments such as lasers or RF microneedling, which carry risk of surface damage, downtime, and side effects, Sofwave delivers controlled fractional ultrasound energy with its integrated Sofcool™ cooling system that protects the skin surface in real time. The result is a safe, effective, and comfortable treatment suitable for all skin types and tones. As the sole distributor in the UAE, Oman, Qatar, and Bahrain, DUBIMED provides full training, clinical support, and after-sales service to integrate Sofwave into your practice with confidence. System Specifications: - Dimensions: 122 × 40 × 40 cm / 48 × 15.75 × 15.75 inches - Weight: ~52 kg / 114.6 lbs - Frequency: 10–12 MHz - Energy: 1–5 J - Electrical Requirements: 100–240 VAC, 50–60 Hz, 8A Max - Handpiece: Solid-state energizer module applicator (no optics, no moving parts, no needles) **Unique features:** 1. SUPERB™ SYNCHRONOUS ULTRASOUND PARALLEL BEAM TECHNOLOGY: Sofwave's core innovation. SUPERB™ simultaneously fires an array of 7 high-intensity, high-frequency ultrasound beams in parallel — without the need for beam focusing. These low-divergence beams have low sensitivity to tissue inhomogeneity, ensuring repeatable and controllable energy deposition at precisely 1.5mm in the mid-dermis every single pulse. This eliminates the variability found in conventional focused ultrasound systems and delivers consistent results across all patients. 2. FRACTIONAL THERMAL EFFECT AT 1.5mm MID-DERMIS: The 7 simultaneous ultrasound beams create an array of unique 3D cylindrical shaped thermal zones in the dermis, separated by regions of completely undamaged tissue — a true fractional effect. The dermal tissue is heated to 60–70°C at exactly 1.5mm depth, triggering neocollagenesis and neoelastogenesis (new collagen and elastin production) in the optimal vector direction relative to skin wrinkles. This targeted depth guarantees no epidermal damage and no harm to underlying nerves, bones, facial fat, or blood vessels. Ultrasound energy is absorbed within 2mm and cannot penetrate deeper. 3. SOFCOOL™ INTEGRATED ACTIVE COOLING SYSTEM: An integrated real-time skin temperature monitoring and active cooling mechanism (Sofcool™) is built directly into the handpiece. This continuously protects the epidermis during energy delivery, ensuring that the thermal effect is accurately directed into the mid-dermis while the skin surface remains safe and comfortable. This is what enables Sofwave to treat all skin types with an exceptional safety profile. 4. TREATS ALL SKIN TYPES AND TONES: Because ultrasound absorption is determined by the microscopic and bulk mechanical properties of tissue — not by skin color or pigmentation — Sofwave is fully suitable for patients across all Fitzpatrick skin types. This sets it apart from light-based technologies (lasers, IPL) which carry risk of pigmentation complications in darker skin tones. 5. FDA CLEARED WITH PROVEN CLINICAL EFFICACY: Sofwave is FDA cleared for the non-invasive treatment of fine lines and wrinkles. In clinical trials using a single treatment protocol, 72% of subjects rated themselves as "improved" to "very improved" on the Global Aesthetic Improvement Scale (GAIS). The majority of patients showed measurable improvement after just one session, with a strong safety profile and no serious adverse events reported. 6. FAST TREATMENT — 30 TO 45 MINUTES: A full-face treatment takes only 30–45 minutes with minimal preparation time. The intuitive interface features simple treatment presets and a large HD touch screen displaying total delivered energy and treatment parameters. Once clinic personnel are trained, the treatment is completely delegatable — physicians do not need to be present for every session. 7. SOLID-STATE ENERGIZER MODULE — NO CONSUMABLES: The handpiece uses a solid-state energizer module with no optics, no moving parts, and no needles. This means no ongoing consumable costs, fast return on investment, and low cost of ownership over the device lifetime. The robust design minimizes maintenance and downtime. 8. COMPLETELY DELEGATABLE TREATMENT: Once trained, clinic staff — not just physicians — can administer the Sofwave treatment. This dramatically improves practice workflow and revenue potential without requiring physician time for every session. 9. NO DOWNTIME — ZERO INTERRUPTION TO DAILY LIFE: Sofwave treatments are non-invasive with no wounds, no injections, and no recovery period. Patients can return to their normal routine immediately. Immediately post-treatment, the skin may appear slightly pink with minimal swelling for up to a few hours, after which it fully resolves. **Clinical indications:** - fine lines - wrinkle reduction - skin tightening - facial lines - facial rejuvenation - anti-aging - collagen stimulation - elastin stimulation - mid-dermis treatment - face lifting - neck tightening - jowl tightening - brow lifting - nasolabial folds - perioral lines - skin laxity - all skin types - all skin tones - non-surgical facelift **Regulatory status:** - FDA-cleared **Positioning:** Also known as: Sofwave SUPERB, Sofwave Medical, SUPERB technology, synchronous ultrasound parallel beam, Sofwave ultrasound, Sofcool device, sofwave treatment. Compared against: Ultherapy, Ulthera, HIFU, MMFU, Ultraformer, Doublo, RF microneedling, Morpheus8, Thermage, laser skin tightening, IPL skin tightening, focused ultrasound facelift. **Clinician FAQs:** **What is Sofwave and what does it treat?** Sofwave is a non-invasive ultrasound device that lifts the eyebrow, submentum, and neck, and improves fine lines and wrinkles. It uses synchronous ultrasound parallel beam (SUPERB) technology delivering energy to the mid-dermis at a consistent 1.5 mm depth. **Is Sofwave approved in the UAE?** Yes. Sofwave carries FDA clearance and is available through DUBIMED, the authorized distributor for the UAE and GCC. Clinics receive MOH-compliant documentation, training, and biomedical service as standard. **What is the ROI profile for a Sofwave purchase?** Sofwave's single-transducer design removes consumable-cartridge overhead per treatment. Most GCC clinics reach breakeven within 40-60 sessions at standard regional pricing. DUBIMED provides a detailed ROI calculator on the product page and during sales consultation. **What is Sofwave?** Sofwave is an FDA-cleared, non-invasive aesthetic device that treats fine lines and wrinkles using SUPERB™ (Synchronous Ultrasound Parallel Beam) technology. It delivers 7 simultaneous high-frequency ultrasound beams to precisely heat the mid-dermis at 1.5mm depth, stimulating the body's natural collagen and elastin production for tighter, smoother, more youthful-looking skin — with no surgery, no downtime, and no needles. **How does Sofwave work?** Sofwave uses SUPERB™ technology — an array of 7 high-intensity, high-frequency (10–12 MHz) ultrasound beams delivered simultaneously in parallel. These beams create 7 unique 3D cylindrical-shaped thermal zones in the mid-dermis at exactly 1.5mm depth, separated by undamaged tissue (a fractional effect). The dermal tissue is heated to 60–70°C, which triggers neocollagenesis (new collagen) and neoelastogenesis (new elastin) in the optimal direction relative to the skin wrinkles. The integrated Sofcool™ cooling system simultaneously protects the epidermis in real time, ensuring no surface damage occurs. **Is Sofwave painful? What does the treatment feel like?** Most patients experience only minimal discomfort during the Sofwave treatment. The sensation is typically described as a mild warmth or brief heat feeling beneath the skin surface as each pulse is delivered. The integrated Sofcool™ active cooling system continuously monitors skin temperature and cools the surface in real time, significantly reducing discomfort compared to non-cooled ultrasound devices. No anesthesia or numbing cream is typically required, making it a very well-tolerated procedure. **When will I see results from Sofwave, and how long do they last?** The collagen and elastin regeneration process stimulated by Sofwave takes time to develop. Most patients see gradual improvements over the 12 weeks following treatment, with optimal results typically visible at the 3-month mark. In clinical trials, some patients noticed early improvement as soon as 2 weeks after their first session. Results are long-lasting — typically 12–18 months — as the body continues to remodel newly produced collagen. Maintenance treatments once every 12–18 months are recommended to sustain results. **How many Sofwave treatments are needed?** Typically, the treatment protocol calls for 1–2 treatments depending on the patient's skin condition, degree of skin laxity, and the treating physician's recommendation. Clinical trials demonstrated meaningful, measurable improvements following a single treatment session, which is a significant advantage over many competing technologies that require 3–6 sessions. Some patients with more advanced skin laxity may benefit from a second session after 3–6 months. **How long does a Sofwave treatment session take?** A full-face Sofwave treatment takes approximately 30–45 minutes. The procedure requires minimal preparation time, and there is no recovery time needed afterward. This fast treatment time is one of Sofwave's key advantages — it easily fits into a patient's lunch break or busy schedule. The straightforward treatment protocol and intuitive interface also mean that once trained, clinic staff can efficiently administer sessions without delays. **Is Sofwave safe? What are the side effects?** Yes. Sofwave is FDA cleared and has a very strong safety profile validated through clinical trials. No serious adverse events were reported in clinical studies. Because the energy targets only the mid-dermis and cannot penetrate beyond 2mm, there is guaranteed protection of the epidermis, underlying nerves, bones, blood vessels, and facial fat. The Sofcool™ integrated cooling mechanism provides an additional layer of real-time epidermal protection. The most common post-treatment observation is mild, transient redness or minimal swelling that resolves within a few hours. **How is Sofwave different from HIFU / Ultherapy / other ultrasound devices?** Sofwave and HIFU devices (like Ultherapy or Ultraformer) both use ultrasound energy for skin tightening, but the core technology and approach are fundamentally different: Depth & Target: Sofwave targets the mid-dermis at exactly 1.5mm. HIFU devices typically target deeper layers — 3mm, 4.5mm (SMAS), or even deeper for body contouring. Sofwave is uniquely optimized for fine lines and wrinkle treatment at the dermis level. Beam Technology: Sofwave uses 7 simultaneous parallel beams (no focusing needed). HIFU uses a single focused beam that converges at a point. The parallel beam approach provides more uniform, repeatable energy deposition. Safety Depth: Sofwave's ultrasound energy is absorbed within 2mm and cannot penetrate deeper — guaranteeing no risk to facial nerves, bones, or fat. HIFU devices penetrate much deeper and require careful placement to avoid nerve injury. Speed: Sofwave treats the full face in 30–45 minutes. HIFU treatments often take longer and involve more discomfort. Consumables: Sofwave uses a solid-state handpiece with no cartridges or consumables. HIFU devices require cartridge replacements. Both technologies stimulate collagen, but they are complementary tools addressing different depths and clinical goals. **What makes Sofwave a good business investment for clinics?** Sofwave offers a compelling business case for aesthetic clinics: 1. No ongoing consumables — the solid-state handpiece requires no cartridge replacements, keeping cost of ownership very low 2. Fast ROI — high patient throughput with 30–45 minute sessions and minimal prep time 3. Delegatable treatment — trained clinic staff (not only physicians) can administer treatments, freeing physician time for higher-value procedures 4. Broad patient base — suitable for all skin types, ages 22+, meaning no patient exclusions based on skin tone 5. Single treatment protocol — many patients achieve results in 1–2 sessions, reducing chair time and increasing patient turnover 6. Proven efficacy — 72% patient satisfaction in clinical trials with a strong safety record supports strong word-of-mouth and patient retention 7. FDA cleared — a strong regulatory credential that supports marketing and patient confidence **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Sofwave™ **Brand:** Sofwave Medical **Type:** medical_device **Portfolio status:** direct portfolio Ultimate Non-Invasive Face Lift & Skin Tightening **Market access:** FDA-cleared. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **Is Sofwave approved in the UAE?** Yes. Sofwave carries FDA clearance and is available through DUBIMED, the authorized distributor for the UAE and GCC. Clinics receive MOH-compliant documentation, training, and biomedical service as standard. ## Product: cosmelan® **Canonical URL:** https://dubaimed.com/products/cosmelan **Brand:** MESOESTETIC ### For patients ### cosmelan® **Learn more:** https://dubaimed.com/products/cosmelan Professional depigmentation method for resistant pigmentation **What it treats:** melasma, hyperpigmentation, discoloration, sun spots, dark spots, post-inflammatory hyperpigmentation, uneven skin tone, chloasma, age spots. **Questions patients commonly ask:** **Does Cosmelan® work on all types of spots?** It is formulated for a wide range of melanocytic pigmentation, including resistant cases. **How long does the treatment last?** The full method typically spans several months, combining in‑clinic and home phases. **When will the results appear?** Visible improvement usually begins within the first few weeks. **Is Cosmelan® a peel?** It is a depigmenting method, not a chemical peel, although exfoliation may occur. **What is the difference between cosmelan® and dermamelan®** dermamelan® is the medical version for more severe or complex pigmentation. **Is cosmelan safe for Fitzpatrick V-VI skin?** Yes. cosmelan is clinically validated across the full Fitzpatrick range and is a first-line choice for melasma in patients of Middle Eastern and South Asian descent. Provider training is required to adapt the protocol to each phototype. **How long does the full cosmelan protocol take?** The in-clinic mask is applied once. Home maintenance with cosmelan 2 cream runs for 6-12 months. Noticeable improvement is typical within 2-3 weeks; full stabilisation of pigmentation is reported at 6 months. **How does cosmelan compare to other depigmentation treatments like chemical peels or laser?** cosmelan offers a significant advantage over chemical peels and laser treatments because it targets melanin production at the cellular level through tyrosinase inhibition, rather than simply removing superficial pigmented layers. This dual-phase approach — an intensive in-clinic mask followed by a home maintenance cream — delivers more consistent and longer-lasting results with lower risk of post-inflammatory hyperpigmentation (PIH), especially on darker skin tones (Fitzpatrick III–VI). Clinical studies show up to 95% pigmentation reduction. Unlike laser, cosmelan can be used year-round with proper sun protection and is suitable for all skin phototypes. **What is cosmelan?** cosmelan is described as a pioneering depigmentation method developed by mesoestetic for visible pigmentation and the cellular mechanisms responsible for melanin overproduction. **What does cosmelan target?** According to the DUBIMED page, it targets visible pigmentation and the underlying cellular mechanisms behind melanin overproduction. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### cosmelan® **URL:** https://dubaimed.com/products/cosmelan **Brand:** MESOESTETIC **Product type:** soft_product **Category:** soft-products **Technical overview:** cosmelan is mesoestetic's world-leading professional depigmentation method, designed to treat and control skin hyperpigmentation including melasma, sun spots, and post-inflammatory hyperpigmentation. The cosmelan method is a two-phase protocol: Phase 1 involves an in-clinic mask application (cosmelan 1) containing a synergistic blend of azelaic acid, kojic acid, phytic acid, retinol, and ascorbic acid that intensively targets melanin synthesis at multiple levels. Phase 2 is a homecare maintenance regimen (cosmelan 2 cream) applied by the patient over several months to sustain results and prevent recurrence. The treatment works by inhibiting tyrosinase enzyme activity — the key catalyst in melanin production — while simultaneously promoting controlled exfoliation and cellular renewal. cosmelan is clinically proven with over 20 years of use worldwide, suitable for all skin types (Fitzpatrick I-VI) and all phototypes, including darker skin tones often difficult to treat. It is the most widely used professional depigmentation method globally with proven efficacy in reducing pigmentation intensity by up to 95%. The protocol requires professional application and patient compliance with a strict homecare routine and sun protection. **Unique features:** World's #1 professional depigmentation method with over 20 years of clinical use and global presence in 80+ countries. Dual-phase protocol combining intensive in-clinic mask (cosmelan 1) with sustained homecare maintenance (cosmelan 2). Multi-target mechanism inhibiting tyrosinase at multiple levels using azelaic acid, kojic acid, phytic acid, retinol, and ascorbic acid. Clinically proven to reduce pigmentation intensity by up to 95%. Safe for all Fitzpatrick skin types (I-VI) including darker phototypes. Continuous action formula that treats existing pigmentation while preventing new melanin formation. No downtime required — patients resume normal activities after mask removal. **Clinical indications:** - melasma - hyperpigmentation - discoloration - sun spots - dark spots - post-inflammatory hyperpigmentation - uneven skin tone - chloasma - age spots **Positioning:** Also known as: dermamelan. Compared against: depigmenting treatment. **Clinician FAQs:** **Can the spots return?** Long‑term control depends on adherence to the full protocol and photoprotection. **Can Cosmelan® be combined with other treatments?** Combination protocols may be recommended by the practitioner based on skin needs. **What is cosmelan and what does it treat?** cosmelan is mesoestetic's flagship pigmentation-management method. It is an in-clinic depigmenting mask applied by a medical professional followed by a structured home maintenance protocol. Indicated for melasma, post-inflammatory hyperpigmentation, and solar lentigines. **Is cosmelan safe for Fitzpatrick V-VI skin?** Yes. cosmelan is clinically validated across the full Fitzpatrick range and is a first-line choice for melasma in patients of Middle Eastern and South Asian descent. Provider training is required to adapt the protocol to each phototype. **How long does the full cosmelan protocol take?** The in-clinic mask is applied once. Home maintenance with cosmelan 2 cream runs for 6-12 months. Noticeable improvement is typical within 2-3 weeks; full stabilisation of pigmentation is reported at 6 months. **How does cosmelan compare to other depigmentation treatments like chemical peels or laser?** cosmelan offers a significant advantage over chemical peels and laser treatments because it targets melanin production at the cellular level through tyrosinase inhibition, rather than simply removing superficial pigmented layers. This dual-phase approach — an intensive in-clinic mask followed by a home maintenance cream — delivers more consistent and longer-lasting results with lower risk of post-inflammatory hyperpigmentation (PIH), especially on darker skin tones (Fitzpatrick III–VI). Clinical studies show up to 95% pigmentation reduction. Unlike laser, cosmelan can be used year-round with proper sun protection and is suitable for all skin phototypes. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### cosmelan® **Brand:** MESOESTETIC **Type:** soft_product **Portfolio status:** direct portfolio Professional depigmentation method for resistant pigmentation **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: Secret Duo **Canonical URL:** https://dubaimed.com/products/secret-duo **Brand:** CLASSYS ### For patients ### Secret Duo **Learn more:** https://dubaimed.com/products/secret-duo Fractional Micro-Needle RF & 1540 Er: Glass Laser **What it treats:** acne scars, surgical scars, stretch marks, fine lines, wrinkles, skin laxity, skin tightening, skin texture improvement, pore reduction, skin rejuvenation, collagen remodeling, active acne, double chin, skin lifting, thread veins, spider veins, depressed scars. **Regulatory status:** FDA-cleared. **Questions patients commonly ask:** **Which areas can be treated with SECRET DUO?** SECRET DUO can treat the face, neck, décolletage, and body, including areas with acne scarring, stretch marks, surgical scars, and texture irregularities. Indications include atrophic acne scars, photodamage, periorbital wrinkles, nasolabial folds, enlarged pores, striae distensae, and post‑inflammatory hyperpigmentation. **Is a SECRET DUO treatment painful?** Most patients experience moderate warmth and pressure during microneedle insertion and brief heat during laser pulses. Discomfort varies by depth, energy settings, and anatomical area. Anaesthetic is typically applied before treatment protocols. **How long does a SECRET DUO session takes?** Sessions range from around 30 minutes for localized facial areas to up to 90 minutes for full‑face combined laser and RF treatments. Cartridge changes, depth adjustments, and multi‑pass protocols are customised based on scar morphology and treatment goals. **When will I see results, and how long do they last?** Initial tightening and texture improvement may appear within 2–4 weeks. Progressive results including scar softening, pore refinement, and wrinkle reduction develop over 3–6 months as neocollagenesis increases. Results typically last 12–18 months depending on skin condition and maintenance protocols. **Is there any downtime after SECRET DUO?** Downtime is minimal compared with ablative resurfacing. Patients may experience redness, mild swelling, pinpoint crusting, and warmth for 2–5 days. Makeup can usually be applied after 24–48 hours, with full social recovery within one week. **Is SECRET DUO suitable for all skin types?** Yes. Both 1540 nm laser and RF technologies target dermal structures without relying on melanin interaction, making SECRET DUO suitable for Fitzpatrick skin types I–VI. Practitioners adjust energy parameters and pulse settings based on phototype and PIH risk. **How does Secret DUO work?** Secret DUO works through two simultaneous non-ablative mechanisms: 1540nm Fractional Er:Glass Laser (superficial-to-mid dermis): Non-ablative laser beams are delivered as multiple micro-columns into the dermis, targeting dermal water to induce collagen heating and dermal remodeling — without ablating or damaging the epidermis. The unique i-Stack function allows up to 10 repetitive stacking passes, deepening the thermal effect with lower energy per pass to maximize collagen stimulation safely. Microneedle Bipolar Fractional RF (0.5mm to 3.5mm depth): Fine medical-grade gold microneedles are inserted to a precisely selected depth and deliver bipolar RF energy directly into the dermis or subcutaneous tissue. This causes coagulation, protein denaturation, and volumetric heating — triggering deep collagen regeneration, skin tightening, and lifting. When used in combination, these two modalities create an amplified synergistic effect — achieving greater skin remodeling than either technology alone, with minimal downtime. **What skin conditions can Secret DUO treat?** Secret DUO is one of the most comprehensive skin remodeling platforms available. It effectively treats: Using the 1540nm Fractional Laser module: - Non-ablative skin resurfacing - Active acne - Atrophic scars (including acne scars) - Wrinkle reduction - Skin lifting and tightening - Skin tone and texture improvement - Pigmentation and sun damage Using the Microneedle RF module: - Non-surgical face lifting - Skin tightening - Wrinkle reduction - Pore reduction - Acne scars - Surgical and traumatic scars - Spider veins and thread veins - Stretch marks and striae - Double chin treatment - Eye bag treatment and tightening - Nasolabial folds, crow's feet Using the optional SmartCure™ add-on: - Thread and spider veins (K3i needle) - Active acne (AC-01 needle) - Depressed scars / subcision (27G–19G needles) **Is Secret DUO treatment safe?** Yes. The Secret RF microneedle component is FDA approved and uses fractional tissue heating — not bulk heating — which means only specific micro-zones of tissue are targeted while surrounding tissue is preserved. Key safety features include: - Variable needle depths (0.5–3.5mm) allow precise targeting with the epidermis specifically protected from heat - Semi-insulated needle design concentrates RF energy at the tip in the dermis, protecting the skin surface - Bipolar RF technology ensures energy stays localized between the two needle poles — no stray current - The 1540nm laser is non-ablative, meaning the skin surface remains intact throughout - 24K gold-plated 32-gauge single-use needles minimize infection risk and ensure uniform energy delivery - Suitable for all skin types including darker Fitzpatrick skin types (no pigmentation risk with RF component) - FDA approval validates its safety profile for clinical use **Is Secret DUO painful?** Comfort depends on the type of procedure and individual pain tolerance, as each person is different. However, Secret DUO was designed with multiple advanced technologies to maximize patient comfort and safety. Topical local anesthetic numbing cream is typically applied 40–60 minutes before the procedure, after which the treatment is very well tolerated by most patients. The 24K gold-coated 32-gauge needles ensure the smoothest possible skin penetration. The i-Stack laser function allows effective results with lower energy per pass, reducing thermal discomfort. **How long does a Secret DUO treatment take?** Treatment time varies depending on the area being treated: - Full face RF microneedling: approximately 15–20 minutes - Adding the neck: approximately 15 additional minutes - Full face using the laser module: approximately 10–30 minutes depending on settings and scan patterns - Numbing cream application prior to the procedure: 40–60 minutes (not treatment time itself) In the Arabic patient brochure, sessions are described as generally taking 10–30 minutes. The exact time depends on the combination of modalities used, the number of passes, and the treatment areas. **How long is the recovery time after Secret DUO?** Secret DUO has minimal downtime due to its non-ablative approach. Expected recovery timeline: - First hour: Initial redness subsides rapidly - 24–36 hours: Redness and swelling typically resolve fully - Occasionally: Some patients may experience redness for a few more days (2–5 days) The skin technology does not cause thermal damage to the skin surface, which is why recovery is faster than ablative treatments. The exact recovery time varies depending on the treatment settings, number of stacks, needle depth, and individual skin sensitivity. **When will I see results from Secret DUO and how long do they last?** Results appear in two phases: Immediate: Some improvement in skin texture and tightening may be visible immediately after the procedure. Gradual (4–6 weeks and beyond): The body continues collagen building for several weeks after the procedure. Most patients see significant improvements in the 4–6 weeks following treatment. With SECRET DUO, patients continue to experience ongoing improvements for up to 6 months after the last treatment session — one of the key clinical advantages of the dual-modality approach. Results shown in clinical photography include: - Acne scars and enlarged pores: visible improvement after 1 treatment - Wrinkle reduction: visible improvement after 1 treatment - Collagen building and pigmentation: visible improvement after combined treatment (2 sessions) - Atrophy scars: visible improvement after combined treatment (2 sessions) - Double chin: visible improvement after 1 treatment **How many Secret DUO treatments are needed?** The number of sessions is variable and will be determined by your doctor based on your treatment goal. General guidance: - Minimum sessions: Many patients see results after just 1 treatment - General recommendation: 1–4 sessions - For maximum clinical benefit: The general consensus is 3 sessions - Session spacing: typically 4–6 weeks apart depending on the indication and skin recovery - Maintenance: 1–2 sessions annually to maintain results Conditions requiring more sessions tend to be deeper concerns like depressed acne scars, significant skin laxity, or stretch marks. Superficial concerns like texture, tone, and early wrinkles often respond well in 1–2 sessions. **What is the SmartCure™ add-on for Secret DUO?** SmartCure™ is an optional thermo-coagulation module that can be added to the Secret DUO system. It uses a smart electro pen with specialized single needles to perform precise thermal coagulation for conditions that benefit from highly localized energy delivery: K3i — Thread and Spider Vein Treatment: An insulated single electrolysis needle (Ø0.075mm) that delivers heating only to the target vein without any risk of damage to the epidermis or surrounding tissue. Ideal for small facial thread veins and spider veins. AC-01 — Acne Treatment: A 1.5mm insulated single needle that smoothly penetrates the skin to generate targeted heating stimulation into the fibroblasts. This improves wrinkles and skin texture through collagen regeneration and rearrangement. Specifically designed for acne treatment. 27G / 22G / 19G — Depressed Scar Subcision: Insulated subcision needles that combine the subcision technique with RF energy. A needle is inserted parallel to and just beneath the skin surface, moving gently between the dermis and subcutaneous tissue to release fibrotic scar adhesions. Provides significant long-term improvement in depressed and pitted acne scars. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Secret Duo **URL:** https://dubaimed.com/products/secret-duo **Brand:** CLASSYS **Product type:** medical_device **Category:** medical-devices **Technical overview:** Secret DUO is the world's only multiplatform non-ablative skin remodeling system that simultaneously combines two technologies in total synergy: a 1540nm Erbium Glass Fractional Laser and a Microneedle Bipolar Fractional RF. Developed by ilooda (Korea) and distributed exclusively in the Middle East by DUBIMED, Secret DUO is the only device on the market that treats all skin layers — from the superficial epidermis to the deep dermis — in a single comprehensive session. The 1540nm Er:Glass fractional laser delivers non-ablative fractional resurfacing by targeting dermal water with multiple laser columns, inducing collagen heating and dermal remodeling without any ablative effect on the epidermis. The advanced microneedle bipolar RF technology simultaneously delivers precisely controlled RF energy to selectively adjusted depths (0.5mm to 3.5mm), providing deeper coagulation, protein denaturation, and volumetric heating for superior skin remodeling. Together, these two complementary modalities create an amplified synergy that achieves clinical results far beyond what either technology could produce alone — with very minimal downtime and side effects. The result: smoother, tighter, more radiant skin with continuous improvement for up to 6 months after the last treatment. Secret DUO is also a My Face My Body 2022 Awards Winner, recognized globally for its innovation and clinical excellence. System Specifications: 1540nm Laser: - Wavelength: 1540nm ±10% - Laser Power: Max 12W ±20% - Pulse Duration: 700μs ~ 5000μs - Energy: 8.4mJ ~ 60.0mJ - Dot Distance: 0.1mm ~ 2.0mm - i-Stack: 1st ~ 10th stacking levels - Treatment Modes: Single, 0.2, 0.5, 0.7, 1.0, 1.5, 2.0s - Treatment Size: Max 10mm × 10mm - Scan Patterns: 5 (Circle, Half Circle L, Half Circle R, Square, Triangle) Microneedle RF: - Output Power: Max 25W ±10% (25-pin) / Max 70W ±10% (64-pin) - Frequency: 2 MHz ±10% - RF Output Time: 50ms ~ 950ms - Delay Time: 100ms ~ 1000ms - Depth: 0.5mm ~ 3.5mm (0.1mm step) - Modes: Single, 0.2s, 0.5s, 0.8s, 1s, 2s (Repeat time) - Intensity: 0 ~ 100% (10 steps) - Electrode: Micro Needle electrode (bipolar) General: - Electrical Power: 100–240 VAC, 50/60 Hz - Needle Quality: Medical grade sterilization, Gold plate, Durable 32-gauge, Single use **Unique features:** 1. THE WORLD'S ONLY DUAL NON-ABLATIVE SYNERGY PLATFORM: Secret DUO is the only device in the world that combines two fully independent non-ablative modalities — 1540nm Er:Glass fractional laser and microneedle bipolar RF — working in total synergy within a single platform. Each technology addresses a different skin layer and mechanism simultaneously: the laser treats the superficial-to-mid dermis via photoacoustic thermal columns, while the RF microneedles deliver volumetric deep-dermal heating. No other device in its class offers this combined amplified dual synergy. 2. 1540nm ERBIUM GLASS NON-ABLATIVE FRACTIONAL LASER: The laser handpiece delivers non-ablative fractional resurfacing by creating multiple micro-columns of thermal coagulation in the dermis, primarily targeting dermal water. The epidermis remains intact (no ablation) while dermal remodeling and collagen synthesis are initiated. Key technical features: - i-Stack function: allows up to 10 repetitive stacking passes to achieve deeper thermal effect with lower energy per pulse — reducing surface damage while maximizing dermal collagen stimulation - 5 customizable scan patterns (Circle, Half Circle L/R, Square, Triangle) with scan size from 1×1mm to 10×10mm and adjustable dot distance (0.1–2.0mm) - Energy range: 8.4mJ to 60.0mJ with pulse durations from 700μs to 5000μs - Multi-sub-pulse delivery: allows deeper penetration with less heat dissipation and less surrounding tissue damage — enabling faster healing 3. MICRONEEDLE BIPOLAR FRACTIONAL RF WITH ADJUSTABLE DEPTH (0.5–3.5mm): The RF handpiece uses advanced bipolar RF technology delivered through fine medical-grade microneedles penetrating to precisely selected depths from 0.5mm to 3.5mm in 0.1mm increments. This enables: - Shallow settings (0.5–1.5mm): superficial dermis treatments — active acne, pores, texture - Mid settings (1.5–2.5mm): mid-dermis — scars, wrinkles, skin laxity - Deep settings (2.5–3.5mm): dermis/subcutaneous junction — skin lifting, subcutaneous fat, double chin The semi-insulated needle design (MTR-AC-C-64 and MTR-AC-C-25) concentrates RF energy at the needle tip in the dermis/subcutaneous tissue, protecting the epidermis from thermal damage. Maximum output: 70W with the 64-pin cartridge. 4. FOUR SPECIALIZED MICRONEEDLE CARTRIDGES: - MTR-AC-C-64: 64-pin semi-insulated | 15×15mm area | Max 70W | Deep dermis/subcutaneous thermal effect - MTR-AC-25: 25-pin non-insulated | 10×10mm area | Max 25W | General/main indications - MTR-AC-C-25: 25-pin semi-insulated | 10×10mm area | Max 25W | Deep dermal/subcutaneous thermal effect - MTR-AC-10: 10-pin non-insulated | 16mm area | Max 25W | Stretch marks, nasolabial folds, crow's feet All needles are medical grade sterilized, 32-gauge, gold-plated, single-use for maximum hygiene and smooth penetration. 5. 24K GOLD NEEDLES — MEDICAL GRADE PRECISION: Secret DUO uses 24K gold-coated 32-gauge microneedles. The gold plating ensures the highest smooth surface quality, minimizing friction during penetration for maximum patient comfort. The durable 32-gauge design enables uniform energy delivery across the entire target area, avoiding uneven coagulation and unwanted damage to surrounding tissue. 6. I-STACK FUNCTION (LASER) — DEEPER EFFECT, LOWER RISK: The i-Stack function (1st to 10th stack) is a repetition stacking feature unique to the 1540nm laser module. It allows the same scan area to be treated multiple times in rapid succession, with each pass delivering additional thermal energy to progressively deeper dermal layers — all with lower energy per pass. This achieves a deeper collagen heating and remodeling effect compared to single high-energy passes, while significantly reducing the risk of epidermal damage and post-treatment downtime. 7. INTELLIGENT I-MOTION TECHNOLOGY: The I-Motion feature enhances RF treatment efficiency by enabling faster needle penetration and continuous energy delivery during movement. This reduces overall session time while maintaining uniform therapeutic results across large treatment areas and improving the overall patient experience and comfort level. 8. SMARTCURE™ OPTIONAL ADD-ON — SINGLE THERMO-COAGULATION: Secret DUO can be optionally equipped with SmartCure™, a smart electro pen for single thermo-coagulation techniques using specialized needles: - K3i (Ø0.075mm insulated needle): treats thread and spider veins by delivering heating only to the target vein without risk of epidermal or surrounding tissue damage - AC-01 (1.5mm insulated needle): penetrates skin to stimulate fibroblasts for wrinkle improvement and skin texture via collagen regeneration and rearrangement — specialized for acne treatment - 27G / 22G / 19G subcision needles: combines subcision technique with RF energy for significant long-term improvement in depressed scars by disrupting fibrotic scar tissue between dermis and subcutaneous tissue 9. USER-FRIENDLY GUI WITH AUTO AND MANUAL MODES: The interface features preset treatment parameters (AUTO mode) for common indications — forehead, face zones — as well as full MANUAL mode for experienced practitioners to customize every parameter. The clear touch-screen interface makes it accessible for all practitioners while allowing expert-level precision. 10. FDA APPROVED & MY FACE MY BODY 2022 AWARD WINNER: Secret RF (the microneedle RF component) is FDA approved, using fractional tissue heating — not bulk heating — making it safe for all skin types including darker Fitzpatrick types. The epidermis is specifically protected from the heat at all treatment depths. Secret DUO was recognized as a My Face My Body 2022 Awards Winner, validating its clinical innovation in the global aesthetics industry. **Clinical indications:** - acne scars - surgical scars - stretch marks - fine lines - wrinkles - skin laxity - skin tightening - skin texture improvement - pore reduction - skin rejuvenation - collagen remodeling - active acne - double chin - skin lifting - thread veins - spider veins - depressed scars **Regulatory status:** - FDA-cleared **Clinician FAQs:** **What is SECRET DUO and how does it work?** SECRET DUO combines 1540 nm Er:Glass fractional laser technology with microneedle RF delivery. The laser creates controlled thermal coagulation columns, while the microneedle RF system delivers high‑frequency energy at adjustable depths to stimulate collagen regeneration and dermal remodelling without epidermal ablation. **Is a SECRET DUO treatment painful?** Most patients experience moderate warmth and pressure during microneedle insertion and brief heat during laser pulses. Discomfort varies by depth, energy settings, and anatomical area. Anaesthetic is typically applied before treatment protocols. **How long does a SECRET DUO session takes?** Sessions range from around 30 minutes for localized facial areas to up to 90 minutes for full‑face combined laser and RF treatments. Cartridge changes, depth adjustments, and multi‑pass protocols are customised based on scar morphology and treatment goals. **When will I see results, and how long do they last?** Initial tightening and texture improvement may appear within 2–4 weeks. Progressive results including scar softening, pore refinement, and wrinkle reduction develop over 3–6 months as neocollagenesis increases. Results typically last 12–18 months depending on skin condition and maintenance protocols. **How many SECRET DUO sessions are recommended?** Protocols often include 3–5 sessions spaced 4–6 weeks apart for acne scars or moderate photoaging. Single sessions may be sufficient for mild texture concerns. Treatment frequency is determined by practitioner assessment and individual response. **Is there any downtime after SECRET DUO?** Downtime is minimal compared with ablative resurfacing. Patients may experience redness, mild swelling, pinpoint crusting, and warmth for 2–5 days. Makeup can usually be applied after 24–48 hours, with full social recovery within one week. **Is SECRET DUO suitable for all skin types?** Yes. Both 1540 nm laser and RF technologies target dermal structures without relying on melanin interaction, making SECRET DUO suitable for Fitzpatrick skin types I–VI. Practitioners adjust energy parameters and pulse settings based on phototype and PIH risk. **Can SECRET DUO be combined with other aesthetic treatments?** SECRET DUO is commonly integrated with chemical peels, subcision, dermal fillers, or platelet‑rich plasma therapy. Combination protocols require appropriate healing intervals of 4–6 weeks. The SmartCure handpiece also supports precise subcision during the same session. **What is Secret DUO?** Secret DUO is the world's only dual non-ablative skin remodeling platform that combines two technologies in one device: a 1540nm Erbium Glass Fractional Laser and a Microneedle Bipolar Fractional RF. Developed by ilooda (Korea) and distributed in the Middle East exclusively by DUBIMED, it is the only treatment that simultaneously works on all skin layers — from the epidermis to the deep dermis — in a single comprehensive session. It is an FDA-approved system and a My Face My Body 2022 Awards Winner. **How does Secret DUO work?** Secret DUO works through two simultaneous non-ablative mechanisms: 1540nm Fractional Er:Glass Laser (superficial-to-mid dermis): Non-ablative laser beams are delivered as multiple micro-columns into the dermis, targeting dermal water to induce collagen heating and dermal remodeling — without ablating or damaging the epidermis. The unique i-Stack function allows up to 10 repetitive stacking passes, deepening the thermal effect with lower energy per pass to maximize collagen stimulation safely. Microneedle Bipolar Fractional RF (0.5mm to 3.5mm depth): Fine medical-grade gold microneedles are inserted to a precisely selected depth and deliver bipolar RF energy directly into the dermis or subcutaneous tissue. This causes coagulation, protein denaturation, and volumetric heating — triggering deep collagen regeneration, skin tightening, and lifting. When used in combination, these two modalities create an amplified synergistic effect — achieving greater skin remodeling than either technology alone, with minimal downtime. **Is Secret DUO treatment safe?** Yes. The Secret RF microneedle component is FDA approved and uses fractional tissue heating — not bulk heating — which means only specific micro-zones of tissue are targeted while surrounding tissue is preserved. Key safety features include: - Variable needle depths (0.5–3.5mm) allow precise targeting with the epidermis specifically protected from heat - Semi-insulated needle design concentrates RF energy at the tip in the dermis, protecting the skin surface - Bipolar RF technology ensures energy stays localized between the two needle poles — no stray current - The 1540nm laser is non-ablative, meaning the skin surface remains intact throughout - 24K gold-plated 32-gauge single-use needles minimize infection risk and ensure uniform energy delivery - Suitable for all skin types including darker Fitzpatrick skin types (no pigmentation risk with RF component) - FDA approval validates its safety profile for clinical use **How long is the recovery time after Secret DUO?** Secret DUO has minimal downtime due to its non-ablative approach. Expected recovery timeline: - First hour: Initial redness subsides rapidly - 24–36 hours: Redness and swelling typically resolve fully - Occasionally: Some patients may experience redness for a few more days (2–5 days) The skin technology does not cause thermal damage to the skin surface, which is why recovery is faster than ablative treatments. The exact recovery time varies depending on the treatment settings, number of stacks, needle depth, and individual skin sensitivity. **How many Secret DUO treatments are needed?** The number of sessions is variable and will be determined by your doctor based on your treatment goal. General guidance: - Minimum sessions: Many patients see results after just 1 treatment - General recommendation: 1–4 sessions - For maximum clinical benefit: The general consensus is 3 sessions - Session spacing: typically 4–6 weeks apart depending on the indication and skin recovery - Maintenance: 1–2 sessions annually to maintain results Conditions requiring more sessions tend to be deeper concerns like depressed acne scars, significant skin laxity, or stretch marks. Superficial concerns like texture, tone, and early wrinkles often respond well in 1–2 sessions. **What is the difference between the 1540nm laser and the microneedle RF in Secret DUO?** The two modalities in Secret DUO complement each other by addressing different skin depths and mechanisms: 1540nm Er:Glass Fractional Laser: - Mechanism: Non-ablative photoacoustic thermal columns targeting dermal water - Depth: Superficial-to-mid dermis (epidermis protected, intact) - Best for: Skin texture, tone, pigmentation, fine lines, active acne, superficial scars, sun damage - Unique feature: i-Stack allows 10 levels of thermal deepening for progressive results Microneedle Bipolar RF: - Mechanism: Mechanical needle penetration + RF energy delivered directly at the needle tip - Depth: 0.5mm to 3.5mm (fully adjustable in 0.1mm steps) - Best for: Deep skin lifting, non-surgical face lifting, deep scars, skin laxity, double chin, stretch marks, spider veins - Unique feature: Variable depth means precise targeting from superficial to subcutaneous tissue When combined: The laser addresses the surface-to-mid dermis while the RF handles the mid-to-deep dermis simultaneously — achieving total skin remodeling from all layers in one session. This synergy is why Secret DUO produces amplified results compared to either modality alone. **What are the 4 microneedle RF cartridges for Secret DUO and when is each used?** Secret DUO comes with 4 specialized microneedle RF cartridges, each designed for specific indications and treatment depths: MTR-AC-C-64 (64-pin semi-insulated): - Treatment area: 15×15mm - Max output: 70W - Semi-insulated design concentrates RF energy at needle tips deep in dermis/subcutaneous tissue - Main use: Cases requiring higher thermal effect at dermis and subcutaneous tissue layers — deep lifting, skin tightening, significant laxity MTR-AC-25 (25-pin non-insulated): - Treatment area: 10×10mm - Max output: 25W - Non-insulated delivers RF along the full needle length - Main use: General/main treatment indications for face and body (most commonly used cartridge) MTR-AC-C-25 (25-pin semi-insulated): - Treatment area: 10×10mm - Max output: 25W - Semi-insulated — focuses energy deeper - Main use: Higher thermal effect at dermis/subcutaneous tissue MTR-AC-10 (10-pin non-insulated): - Treatment area: 16mm - Max output: 25W - Fewer pins for precise linear treatment - Main use: Stretch marks, nasolabial folds, crow's feet — smaller or linear areas requiring targeted precision All cartridges use 32-gauge gold-plated single-use needles for maximum safety and comfort. **How does Secret DUO compare to standalone RF microneedling devices like Morpheus8?** Secret DUO and standalone RF microneedling devices (like Morpheus8) both use microneedle RF for deep skin remodeling, but Secret DUO offers several important advantages: 1. Dual Technology: Secret DUO adds a full 1540nm Er:Glass fractional laser module — treating the superficial dermis, pigmentation, active acne, and skin texture simultaneously. Morpheus8 has no laser component. 2. Wider Indication Range: The laser addresses conditions that RF alone cannot treat effectively — active acne, pigmentation, sun damage, fine surface texture — while the RF handles the deep lifting and scar remodeling. One device covers what would otherwise require two. 3. Amplified Synergy: When both modalities are used together, the clinical outcome exceeds what either could achieve alone. The combined thermal effect from two different mechanisms creates deeper, more comprehensive collagen remodeling. 4. SmartCure™ Option: The optional thermo-coagulation module adds thread vein treatment, acne treatment, and subcision for depressed scars — expanding the clinical capability further. 5. Depth Range: Secret DUO RF goes from 0.5mm to 3.5mm in 0.1mm steps — comparable to or deeper than most competitors. 6. Award Recognition: My Face My Body 2022 Award Winner — validated by industry peers. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Secret Duo **Brand:** CLASSYS **Type:** medical_device **Portfolio status:** direct portfolio Fractional Micro-Needle RF & 1540 Er: Glass Laser **Market access:** FDA-cleared. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **What is Secret DUO?** Secret DUO is the world's only dual non-ablative skin remodeling platform that combines two technologies in one device: a 1540nm Erbium Glass Fractional Laser and a Microneedle Bipolar Fractional RF. Developed by ilooda (Korea) and distributed in the Middle East exclusively by DUBIMED, it is the only treatment that simultaneously works on all skin layers — from the epidermis to the deep dermis — in a single comprehensive session. It is an FDA-approved system and a My Face My Body 2022 Awards Winner. ## Product: Volnewmer **Canonical URL:** https://dubaimed.com/products/volnewmer **Brand:** CLASSYS ### For patients ### Volnewmer **Learn more:** https://dubaimed.com/products/volnewmer Monopolar Radiofrequency Technology **What it treats:** skin lifting, skin tightening, face lifting, facial contouring, volume restoration, collagen regeneration, wrinkle reduction, fine lines, skin laxity, body contouring, body tightening, abdomen tightening, arm tightening, thigh tightening, eye area treatment, periorbital tightening, jawline, jowl, neck lifting, overall rejuvenation, skin texture improvement, pore reduction, skin tone improvement, sagging skin. **Questions patients commonly ask:** **Which areas can be treated with Volnewmer?** Volnewmer can be used on the face, neck, décolletage, and body including the abdomen, arms, thighs, buttocks, bra‑line, knees, and elbows. Indications include mild to moderate laxity, fine lines, jawline and submental concerns, enlarged pores, uneven texture, and postpartum or weight‑loss related looseness. **Is Volnewmer treatment painful?** Most patients report mild warmth or tingling during treatment. The four‑step cooling system stabilises applicator temperature and reduces discomfort compared with earlier RF systems. **How long does Volnewmer session takes?** Session duration varies by area. Smaller facial zones typically require around 20 minutes, while larger body regions may take up to 45 minutes. Practitioners adjust protocols based on indication, coverage, and patient‑specific factors. **When Will I See Results And How Long Do They Last?** Initial tightening may be felt immediately after treatment. More defined results develop over 4–8 weeks as new collagen forms and are often maintained for 6–12 months depending on skin condition and lifestyle. **IS THERE ANY DOWNTIME AFTER VOLNEWMER?** Downtime is minimal. Temporary redness or warmth may occur and typically resolves within a few hours, allowing same‑day return to normal activities. **IS VOLNEWMER SUITABLE FOR ALL SKIN TYPES?** Volumetric monopolar RF is suitable for a wide range of skin types because it targets deeper dermal layers without relying on chromophore interaction. Practitioners adjust settings based on individual skin characteristics and medical history. **What is Volnewmer?** Volnewmer is an advanced non-invasive monopolar radiofrequency (RF) device developed by CLASSYS for high-intensity skin lifting, tightening, and volume restoration. It operates at 6.78 MHz — a higher and safer RF frequency — and uses patented Curved Surface and Hidden Edge tip technology to deliver powerful collagen regeneration with minimal pain and no downtime. The slogan "Volume Up New You®" reflects its unique ability to not just tighten skin but actually restore lost collagen volume in the dermis — reversing one of the core effects of facial aging. **What makes Volnewmer different from other RF devices like Thermage?** Volnewmer differentiates itself from conventional monopolar RF devices (such as Thermage) in several important ways: 1. Curved Surface & Hidden Edge Tips: Standard RF tips have flat surfaces that concentrate energy at the edges, causing edge burns and pain. Volnewmer's curved tip surface distributes heat evenly across the entire dermis contact area — enabling higher energy delivery with less discomfort. 2. Real-Time Impedance Safety System: Volnewmer stops firing automatically if the tip loses full skin contact. Most RF devices do not have this real-time cutoff mechanism. 3. 4-Step Vibration + Cooling: Built-in vibration desensitizes tissue before each shot. Thermage uses a tip-cooling mechanism but not vibration-assisted pain control. 4. 4 Specialized Tips including I-TIP for the eye area — most competitors offer 1–2 tips only. 5. No Time Lock + Dual Handpieces: Combine multiple areas in one session and switch handpieces without stopping. 6. Volume Restoration: Clinically proven 3D volumetric improvement (17+ cc at 3 months) — not just tightening but actual volume replenishment. 7. Cost-effective consumables: Each tip provides 3,000–6,000 shots at a reasonable cost per consumable. **What areas of the face and body can Volnewmer treat?** Volnewmer is one of the most comprehensive RF platforms available, treating both facial and body areas with its 4 specialized tips: Face & Eye Area (I-TIP + F-TIP + V-TIP): - Periorbital area / eye area (I-TIP 0.25 — the only tip designed specifically for this delicate zone) - Forehead, cheeks, jawline, jowls, chin - Nasolabial folds and perioral lines - Neck and submental area Face & Body (V-TIP 4.0): - All facial areas - Arms, inner arms - Décolletage and chest Large Body Areas (S-TIP 16.0): - Abdomen and stomach - Thighs (inner and outer) - Flanks / love handles - Upper arms - Buttocks - Knees This makes Volnewmer suitable for comprehensive full-body treatment in a single device. **Is Volnewmer painful?** Volnewmer is designed to be one of the most comfortable RF treatment experiences available, despite operating at high energy levels. This is achieved through: 1. Curved Surface Tip Design: Even heat distribution eliminates the painful edge-concentration effect of flat tips 2. Hidden Edge Technology: Removes the overheating at tip perimeters that causes burning sensations 3. 4-Step Vibration System: The built-in vibration desensitizes skin nerve endings before and during energy delivery 4. Continuous Epidermal Cooling: Protects the skin surface and reduces perceived heat The result is that despite being treated with high energy levels, Volnewmer has relatively minimal side effects and pain during the procedure. Some people may experience minor warmth or a brief prickling sensation. Mild swelling or redness may appear immediately after treatment but typically subsides within 24 hours. **Is there any downtime after Volnewmer treatment?** No. There is no downtime required after a Volnewmer treatment. Your face will appear normal after the procedure, and your skin will feel a little smoother right away. Since Volnewmer is a completely non-surgical method for skin tightening and lifting, patients can return to their normal daily activities immediately. Some patients may experience mild, temporary redness or slight swelling, but these side effects typically subside within 24 hours. No special aftercare routine or recovery period is required. **When will I see results from Volnewmer and how long do they last?** Results from Volnewmer appear in two phases: Immediate (same day): Some patients notice an immediate tightening effect from the collagen contraction caused by the RF thermal energy. Gradual (2–6 months): For most patients, measurable results appear gradually in the 2 to 6 months following a treatment session as new collagen is regenerated and remodeled. This is the primary improvement phase where volume restoration and skin quality improvement become most visible. Clinical evidence (VECTRA 3D camera analysis) showed: - 17.43 cc total facial volume increase at 3 months post-treatment - 14.42 cc volume increase at 5 months post-treatment - Improvements across volume (74%), texture (58%), spots (53%), wrinkles (53%), pores (53%), and red areas (53%) How long results last: Results can last years, depending on your skin condition and the natural aging process. Volnewmer does not stop aging but does slow it down. Maintenance sessions are recommended annually or as advised by your practitioner. **What is the 4-tip system in Volnewmer and which tip is for which area?** Volnewmer comes with 4 purpose-engineered interchangeable tips, each optimized for a specific treatment zone: I-TIP 0.25 cm² (Green — Eye Area): The smallest and most delicate tip, specifically engineered for the periorbital (around the eye) zone, crow's feet, and under-eye areas. Allows safe RF treatment in areas too sensitive or small for standard tips. F-TIP 3.0 cm² (Purple/Blue — Face): Designed for facial contouring and tightening. Used on cheeks, jawline, chin, forehead, nasolabial folds, perioral area, and neck. Ideal for detailed facial work. V-TIP 4.0 cm² (Pink — Face & Body): A versatile mid-size tip suitable for both facial and body treatments. Can be used for larger facial areas as well as smaller body zones like upper arms and décolletage. S-TIP 16.0 cm² (Gold — Body): The largest tip, designed for efficient coverage of large body areas. Used for abdomen, thighs, flanks, upper arms, buttocks, and knees. The large surface area makes body treatments significantly faster. **What are the clinical results of Volnewmer?** Volnewmer has published clinical results measured using VECTRA 3D camera analysis — one of the most objective clinical measurement tools available — demonstrating quantifiable improvements across multiple skin parameters: Volume Restoration (the unique differentiator): - 17.43 cc total facial volume increase at 3 months post-treatment (Patient Case 1) - 14.42 cc total facial volume increase at 5 months post-treatment (Patient Case 2) - 74% of patients showed measurable volume improvement Skin Quality Improvements (Vectra 3D Report): - 58% showed improvement in skin texture - 53% showed improvement in spots - 53% showed improvement in wrinkles - 53% showed improvement in pores - 53% showed improvement in red areas Clinical photos across multiple patients show measurable lifting and tightening at 8 weeks and 12 weeks post-treatment when compared to baseline, with continued improvement visible at 3 months. These results were observed across both male and female patients with different skin types. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Volnewmer **URL:** https://dubaimed.com/products/volnewmer **Brand:** CLASSYS **Product type:** medical_device **Category:** medical-devices **Technical overview:** VOLNEWMER is the world's most advanced non-invasive monopolar radiofrequency (RF) treatment system for high-intensity skin lifting, tightening, and contouring through rejuvenation. Developed by CLASSYS — the global medical aesthetics pioneer behind the Ultraformer series — Volnewmer combines 6.78 MHz high-frequency RF energy with innovative tip engineering to deliver exceptional clinical results with minimal side effects and no downtime. The name says it all: VOLUME UP NEW YOU®. Volnewmer uniquely delivers not just skin tightening and lifting but actual volumetric restoration — rebuilding lost collagen volume in the dermis to restore the youthful facial structure that has been diminished by aging. Volnewmer features 4 interchangeable treatment tips (I-Tip, F-Tip, V-Tip, S-Tip) covering the eye area, face, face & body, and large body areas respectively — making it a truly comprehensive single-platform solution. Its patented Curved Surface and Hidden Edge tip design, combined with a Real-Time Impedance Detecting System and 4-step Vibration & Cooling system, set it apart from every other RF device on the market. System Specifications: - RF Frequency: 6.78 MHz - Treatment Range: Max. 16 cm² - Display: 10.1 inch LCD touch screen - Voltage/Frequency: 220–240 VAC, 50/60 Hz - Power Consumption (Maximum Output): 1600 VA - Handpieces: 2 (dual handpiece system with continuous cooling) - Tips: 4 interchangeable tips (3,000–6,000 shots per consumable) **Unique features:** 1. 6.78 MHz MONOPOLAR RF — HIGHER BUT SAFER FREQUENCY: Volnewmer operates at 6.78 MHz — a higher radiofrequency than most RF devices — which enables deeper, more uniform energy penetration into the dermis while actually reducing the risk of surface burns or pain. At this frequency, the RF energy is transmitted more evenly and safely through tissue, maximizing collagen regeneration in the dermis without concentrating harmful heat at the skin surface. 2. CURVED SURFACE & HIDDEN EDGE TIP DESIGN (PATENTED): This is Volnewmer's most critical safety and performance innovation. Conventional RF tips have flat surfaces where energy concentrates at the edges, causing overheating and pain at the tip perimeter. Volnewmer's Curved Surface Tip Design distributes thermal energy evenly across the entire tip surface in the dermis. The Hidden Edge Design moves the tip edge inward, eliminating the edge-concentration effect entirely. The result: high-energy RF treatment with dramatically reduced side effects and pain — enabling practitioners to work at clinically effective energy levels that were previously uncomfortable for patients. 3. REAL-TIME IMPEDANCE DETECTING SYSTEM: A proprietary safety mechanism that continuously monitors the electrical impedance between the tip and the skin. The system requires full tip-to-skin contact to deliver a complete shot. If the tip lifts off the skin even slightly, the operation stops immediately and automatically. This prevents accidental energy delivery to incorrect tissue depths and ensures every shot is delivered at precisely the right contact — protecting both patient safety and treatment consistency. 4. 4-STEP VIBRATION & COOLING SYSTEM FOR PAINLESS TREATMENT: Volnewmer integrates a 4-level vibration mechanism alongside its continuous epidermal cooling system directly into the tips. The vibration desensitizes the nerve endings at the treatment area, reducing the perception of heat and discomfort. The simultaneous cooling protects the epidermis surface. Together, these create a significantly more comfortable treatment experience, allowing higher energy levels to be used safely — translating directly to better clinical outcomes. 5. 4 SPECIALIZED INTERCHANGEABLE TIPS: Volnewmer is a comprehensive platform with 4 purpose-engineered tips: - I-TIP 0.25 cm² (Eye Area — green): The smallest tip, precisely designed for the delicate periorbital zone and areas around the eyes - F-TIP 3.0 cm² (Face — purple/blue): Optimized for facial contouring, cheeks, forehead, and perioral areas - V-TIP 4.0 cm² (Face & Body — pink): Versatile tip for both facial and body treatments - S-TIP 16.0 cm² (Body — gold): The largest tip for treating large body areas such as abdomen, thighs, arms, and flanks Each tip is designed with the curved surface and hidden edge technology, and each consumable provides 3,000–6,000 shots depending on the tip type. 6. DUAL HANDPIECE SYSTEM: Volnewmer features 2 handpieces with a continuous cooling system. The dual handpiece setup significantly reduces the hassle of changing cartridges mid-treatment and enables physicians to switch between tip sizes without interrupting the clinical workflow. This adds convenience for physicians treating multiple areas in a single session. 7. NO TIME LOCK SYSTEM: Physicians can combine different treatments in a single session through Volnewmer's no-time-lock system. This means multiple areas, multiple tip types, and multiple treatment goals can be addressed in one visit — maximizing patient value and clinic efficiency. 8. VOLUME RESTORATION — UNIQUE COLLAGEN REBUILDING: Unlike most RF or HIFU devices that focus purely on tightening and lifting, Volnewmer is clinically proven to produce volumetric improvement. Clinical data using VECTRA 3D camera analysis confirmed a total of 17.43 cc volume increase at 3 months and 14.42 cc increase at 5 months post-treatment. 74% of patients showed improvement in volume, 58% in texture, 53% in spots/wrinkles/pores/red areas according to the Vectra 3D clinical study. This volumetric collagen rebuilding — replicating the effect of collagen volume loss reversal — is what makes Volnewmer truly unique in the monopolar RF space. 9. AUTO ENERGY ADJUSTMENT: Before each shot is fired, the system automatically adjusts the energy output to ensure that thermal energy is uniformly transmitted to the skin according to the defined energy level. This eliminates variability caused by operator technique or skin contact inconsistency, ensuring every shot delivers the same precise therapeutic dose. **Clinical indications:** - skin lifting - skin tightening - face lifting - facial contouring - volume restoration - collagen regeneration - wrinkle reduction - fine lines - skin laxity - body contouring - body tightening - abdomen tightening - arm tightening - thigh tightening - eye area treatment - periorbital tightening - jawline - jowl - neck lifting - overall rejuvenation - skin texture improvement - pore reduction - skin tone improvement - sagging skin **Positioning:** Also known as: Volnewmer, Vol Newmer, VOLNEWMER, Volume Up New You, CLASSYS RF, Volnewmer RF, 6.78MHz RF device, Volnewmer CLASSYS. Compared against: Thermage, Thermage FLX, monopolar RF, Solta Medical, Venus Legacy, Profound RF, Morpheus8, RF microneedling, InMode, Fractora, radiofrequency lifting, RF facelift. **Clinician FAQs:** **What is Volnewmer and how does it work?** Volnewmer is a non‑invasive monopolar radiofrequency device operating at 6.78 MHz to deliver controlled thermal energy into the upper and lower dermis. This volumetric heating stimulates collagen remodelling and improves elasticity, while real‑time impedance monitoring and water cooling protect the epidermis during treatment. **Is Volnewmer treatment painful?** Most patients report mild warmth or tingling during treatment. The four‑step cooling system stabilises applicator temperature and reduces discomfort compared with earlier RF systems. **How long does Volnewmer session takes?** Session duration varies by area. Smaller facial zones typically require around 20 minutes, while larger body regions may take up to 45 minutes. Practitioners adjust protocols based on indication, coverage, and patient‑specific factors. **HOW MANY VOLNEWMER SESSIONS ARE RECOMMENDED?** The number of sessions depends on indication, baseline laxity, and treatment goals. Many protocols use a short series of treatments followed by periodic maintenance. **Can Volnewmer Be Combined With Other Aesthetic Treatments?** Yes. Volnewmer is commonly combined with other aesthetic procedures such as injectables, thread lifting, and additional energy based devices. It is also frequently used to maintain and enhance results following lifting and contouring treatments when performed with appropriate timing and intervals. For optimal outcomes, Volnewmer is highly recommended in combination with Ultraformer MPT. This advanced pairing, known as the Volformer protocol, combines monopolar RF skin tightening with focused ultrasound lifting to address both skin quality and deeper structural support. When used together, Volnewmer and Ultraformer MPT work synergistically to maximize tightening, lifting, and long term rejuvenation results. **What is Volnewmer?** Volnewmer is an advanced non-invasive monopolar radiofrequency (RF) device developed by CLASSYS for high-intensity skin lifting, tightening, and volume restoration. It operates at 6.78 MHz — a higher and safer RF frequency — and uses patented Curved Surface and Hidden Edge tip technology to deliver powerful collagen regeneration with minimal pain and no downtime. The slogan "Volume Up New You®" reflects its unique ability to not just tighten skin but actually restore lost collagen volume in the dermis — reversing one of the core effects of facial aging. **How does Volnewmer work?** Volnewmer delivers 6.78 MHz monopolar radiofrequency energy through its specialized tips directly into the dermal layer. The RF thermal energy causes two key biological effects: 1. Collagen Re-Structure: The heat causes existing collagen strands to contract and re-tighten immediately, providing an initial lifting effect 2. Collagen Re-Generation: The controlled thermal injury triggers accelerated extracellular matrix-enhanced collagen regeneration over the following weeks and months, progressively improving skin firmness, volume, and texture The Auto Energy Adjustment system ensures that before each shot, the energy output is calibrated so thermal energy is uniformly transmitted to the dermis at the defined therapeutic level — every time, without variation. **What makes Volnewmer different from other RF devices like Thermage?** Volnewmer differentiates itself from conventional monopolar RF devices (such as Thermage) in several important ways: 1. Curved Surface & Hidden Edge Tips: Standard RF tips have flat surfaces that concentrate energy at the edges, causing edge burns and pain. Volnewmer's curved tip surface distributes heat evenly across the entire dermis contact area — enabling higher energy delivery with less discomfort. 2. Real-Time Impedance Safety System: Volnewmer stops firing automatically if the tip loses full skin contact. Most RF devices do not have this real-time cutoff mechanism. 3. 4-Step Vibration + Cooling: Built-in vibration desensitizes tissue before each shot. Thermage uses a tip-cooling mechanism but not vibration-assisted pain control. 4. 4 Specialized Tips including I-TIP for the eye area — most competitors offer 1–2 tips only. 5. No Time Lock + Dual Handpieces: Combine multiple areas in one session and switch handpieces without stopping. 6. Volume Restoration: Clinically proven 3D volumetric improvement (17+ cc at 3 months) — not just tightening but actual volume replenishment. 7. Cost-effective consumables: Each tip provides 3,000–6,000 shots at a reasonable cost per consumable. **When will I see results from Volnewmer and how long do they last?** Results from Volnewmer appear in two phases: Immediate (same day): Some patients notice an immediate tightening effect from the collagen contraction caused by the RF thermal energy. Gradual (2–6 months): For most patients, measurable results appear gradually in the 2 to 6 months following a treatment session as new collagen is regenerated and remodeled. This is the primary improvement phase where volume restoration and skin quality improvement become most visible. Clinical evidence (VECTRA 3D camera analysis) showed: - 17.43 cc total facial volume increase at 3 months post-treatment - 14.42 cc volume increase at 5 months post-treatment - Improvements across volume (74%), texture (58%), spots (53%), wrinkles (53%), pores (53%), and red areas (53%) How long results last: Results can last years, depending on your skin condition and the natural aging process. Volnewmer does not stop aging but does slow it down. Maintenance sessions are recommended annually or as advised by your practitioner. **How many Volnewmer sessions are needed?** The number of sessions varies based on the treatment area, skin condition, degree of laxity, and individual goals. Generally: - For facial lifting and tightening: 1–3 sessions are typically recommended, spaced 4–8 weeks apart - For body contouring (abdomen, thighs, arms): 2–4 sessions may be needed for optimal results - Maintenance: Annual or biannual sessions are recommended to maintain and extend results Your practitioner will assess your skin during a consultation and design a customized treatment plan based on your specific needs and desired outcomes. **What is the Real-Time Impedance Detecting System in Volnewmer?** The Real-Time Impedance Detecting System is a proprietary safety technology built into Volnewmer that continuously monitors the electrical impedance (resistance) between the treatment tip and the patient's skin during the procedure. How it works: The system requires that the tip be in complete, full contact with the skin to successfully fire and complete a shot. If the tip partially or fully lifts off the skin — even momentarily — the system immediately detects the change in impedance and stops the operation automatically. Why it matters: This prevents accidental delivery of RF energy to incorrect tissue layers (which could cause burns or unintended effects) and ensures every single shot is delivered at the correct depth and uniform contact. It is a critical safety feature that protects patients during high-energy RF treatment and ensures consistent, reproducible clinical outcomes regardless of operator experience. **What are the clinical results of Volnewmer?** Volnewmer has published clinical results measured using VECTRA 3D camera analysis — one of the most objective clinical measurement tools available — demonstrating quantifiable improvements across multiple skin parameters: Volume Restoration (the unique differentiator): - 17.43 cc total facial volume increase at 3 months post-treatment (Patient Case 1) - 14.42 cc total facial volume increase at 5 months post-treatment (Patient Case 2) - 74% of patients showed measurable volume improvement Skin Quality Improvements (Vectra 3D Report): - 58% showed improvement in skin texture - 53% showed improvement in spots - 53% showed improvement in wrinkles - 53% showed improvement in pores - 53% showed improvement in red areas Clinical photos across multiple patients show measurable lifting and tightening at 8 weeks and 12 weeks post-treatment when compared to baseline, with continued improvement visible at 3 months. These results were observed across both male and female patients with different skin types. **What is the No Time Lock system in Volnewmer and why is it important for clinics?** The No Time Lock system means there is no session time restriction imposed on the device. Physicians can freely combine different tips and treat multiple areas — face, neck, and body — all in a single patient session without being constrained by a timer or usage limit. Why it matters for clinics: 1. Comprehensive single-session treatments: A patient can have their full face, neck, and a body area treated in one visit 2. Better patient value: More areas treated per visit increases the value and satisfaction of each appointment 3. Increased revenue per session: More treatment areas per visit directly impacts clinic revenue 4. No artificial restrictions: Practitioners can focus entirely on clinical protocol rather than managing device timers 5. Cost-effective consumables: Depending on the tip, each consumable provides 3,000–6,000 shots, making per-shot costs very competitive compared to alternatives **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Volnewmer **Brand:** CLASSYS **Type:** medical_device **Portfolio status:** direct portfolio Monopolar Radiofrequency Technology **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **What makes Volnewmer different from other RF devices like Thermage?** Volnewmer differentiates itself from conventional monopolar RF devices (such as Thermage) in several important ways: 1. Curved Surface & Hidden Edge Tips: Standard RF tips have flat surfaces that concentrate energy at the edges, causing edge burns and pain. Volnewmer's curved tip surface distributes heat evenly across the entire dermis contact area — enabling higher energy delivery with less discomfort. 2. Real-Time Impedance Safety System: Volnewmer stops firing automatically if the tip loses full skin contact. Most RF devices do not have this real-time cutoff mechanism. 3. 4-Step Vibration + Cooling: Built-in vibration desensitizes tissue before each shot. Thermage uses a tip-cooling mechanism but not vibration-assisted pain control. 4. 4 Specialized Tips including I-TIP for the eye area — most competitors offer 1–2 tips only. 5. No Time Lock + Dual Handpieces: Combine multiple areas in one session and switch handpieces without stopping. 6. Volume Restoration: Clinically proven 3D volumetric improvement (17+ cc at 3 months) — not just tightening but actual volume replenishment. 7. Cost-effective consumables: Each tip provides 3,000–6,000 shots at a reasonable cost per consumable. **Is Volnewmer painful?** Volnewmer is designed to be one of the most comfortable RF treatment experiences available, despite operating at high energy levels. This is achieved through: 1. Curved Surface Tip Design: Even heat distribution eliminates the painful edge-concentration effect of flat tips 2. Hidden Edge Technology: Removes the overheating at tip perimeters that causes burning sensations 3. 4-Step Vibration System: The built-in vibration desensitizes skin nerve endings before and during energy delivery 4. Continuous Epidermal Cooling: Protects the skin surface and reduces perceived heat The result is that despite being treated with high energy levels, Volnewmer has relatively minimal side effects and pain during the procedure. Some people may experience minor warmth or a brief prickling sensation. Mild swelling or redness may appear immediately after treatment but typically subsides within 24 hours. **Can Volnewmer treat the eye area safely?** Yes — Volnewmer is specifically equipped with the I-TIP 0.25 cm², a micro-tip designed exclusively for the periorbital (eye area) zone. This tiny tip (0.25 cm²) allows precise, controlled RF energy delivery to the delicate skin around the eyes — including crow's feet, under-eye area, and the upper eyelid skin — areas that are too sensitive for standard RF tips. The combination of the I-TIP's small surface, the Curved Surface & Hidden Edge design for even energy distribution, the Real-Time Impedance safety cutoff, and the Vibration + Cooling comfort system makes Volnewmer one of the very few RF platforms that can safely and comfortably treat the periorbital region. Most RF devices specifically exclude eye area treatment due to safety concerns. ## Product: dermamelan® intimate **Canonical URL:** https://dubaimed.com/products/dermamelan-intimate **Brand:** MESOESTETIC ### For patients ### dermamelan® intimate **Learn more:** https://dubaimed.com/products/dermamelan-intimate Professional depigmentation method for intimate‑area hyperpigmentation **What it treats:** intimate discoloration, pigment control, intimate area hyperpigmentation, genital darkening, underarm darkening, inner thigh pigmentation, perianal darkening, friction-induced pigmentation, hormonal intimate darkening. **Questions patients commonly ask:** **What areas can be treated?** Genital‑perineal region, perianal area, mons pubis, inner thighs, and groin. **How soon will I see results?** Visible improvement typically appears after the first session. **Is the treatment safe for sensitive skin** Yes. The method is formulated specifically for intimate‑area tissue. **Is the treatment available for home use?** No. The professional method must be performed in‑clinic. **Is dermamelan intimate safe for sensitive areas and what results can patients expect?** dermamelan intimate has been specifically formulated and clinically tested for use on sensitive body areas including the axillary, inguinal, perianal, and genital regions. The formula accounts for the thinner, more delicate skin in these zones with adjusted concentrations that minimize irritation while maintaining strong depigmenting efficacy. Patients typically see a noticeable reduction in hyperpigmentation within 3–4 weeks, with optimal results achieved over 2–3 months of the home maintenance phase. The treatment is safe for all skin phototypes and both men and women. Mild, temporary redness and sensitivity in the treated area are normal and resolve within a few days. **What is dermamelan intimate used for?** dermamelan intimate is formulated to address intimate-area hyperpigmentation influenced by factors such as aging, genetics, friction, depilation, hormonal changes, and lifestyle factors. **How does dermamelan intimate approach the concern?** The DUBIMED page explains that it combines targeted depigmenting activity with support for the intimate-area skin environment. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### dermamelan® intimate **URL:** https://dubaimed.com/products/dermamelan-intimate **Brand:** MESOESTETIC **Product type:** soft_product **Category:** soft-products **Technical overview:** dermamelan intimate is mesoestetic's specialized professional depigmentation treatment designed exclusively for hyperpigmentation in intimate and sensitive body areas. It addresses unwanted darkening of the genital area, inner thighs, perianal region, and axillary (underarm) zones — conditions that are common but underserved in aesthetic dermatology. The treatment follows a professional dual-phase protocol: Phase 1 is an in-clinic application of the dermamelan intimate mask containing a carefully calibrated blend of depigmenting actives including azelaic acid, kojic acid, phytic acid, and niacinamide at concentrations optimized for the thinner, more sensitive skin of intimate areas. Phase 2 is a homecare maintenance cream applied by the patient over several weeks to consolidate and maintain results. The formulation specifically accounts for the unique characteristics of intimate-area skin — higher sensitivity, different melanocyte density, friction-induced pigmentation triggers, and hormonal influences. dermamelan intimate is clinically tested for safety and efficacy on mucosal-adjacent skin. It is suitable for all skin types and phototypes, and addresses pigmentation caused by hormonal changes, friction, aging, post-inflammatory responses, and hair removal methods. The treatment offers a non-invasive, non-surgical alternative to intimate-area lightening procedures. **Unique features:** First and only professional depigmentation method specifically developed for intimate and sensitive body areas. Formulated with concentrations calibrated for thinner, mucosal-adjacent skin with higher sensitivity profiles. Addresses underserved aesthetic concern — intimate-area hyperpigmentation — with a clinically tested, safe protocol. Dual-phase professional method (in-clinic mask + homecare maintenance) adapted from the proven dermamelan technology. Contains azelaic acid, kojic acid, phytic acid, and niacinamide in intimate-area-optimized concentrations. Non-invasive alternative to surgical or laser intimate lightening procedures. Treats multiple causes of intimate darkening: hormonal, friction, post-inflammatory, aging, and hair removal-related. **Clinical indications:** - intimate discoloration - pigment control - intimate area hyperpigmentation - genital darkening - underarm darkening - inner thigh pigmentation - perianal darkening - friction-induced pigmentation - hormonal intimate darkening **Clinician FAQs:** **Why is a home phase required?** It maintains depigmenting activity and supports long‑term regulation. **Can the treatment prevent recurrence?** It helps regulate melanin production, reducing the likelihood of future darkening. **Is dermamelan intimate safe for sensitive areas and what results can patients expect?** dermamelan intimate has been specifically formulated and clinically tested for use on sensitive body areas including the axillary, inguinal, perianal, and genital regions. The formula accounts for the thinner, more delicate skin in these zones with adjusted concentrations that minimize irritation while maintaining strong depigmenting efficacy. Patients typically see a noticeable reduction in hyperpigmentation within 3–4 weeks, with optimal results achieved over 2–3 months of the home maintenance phase. The treatment is safe for all skin phototypes and both men and women. Mild, temporary redness and sensitivity in the treated area are normal and resolve within a few days. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### dermamelan® intimate **Brand:** MESOESTETIC **Type:** soft_product **Portfolio status:** direct portfolio Professional depigmentation method for intimate‑area hyperpigmentation **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: Etherea MX **Canonical URL:** https://dubaimed.com/products/etherea-mx **Brand:** VYDENCE ### For patients ### Etherea MX **Learn more:** https://dubaimed.com/products/etherea-mx Universal laser and light-based platform **What it treats:** skin rejuvenation, pigmentation, laser procedures, melasma, acne scars, vascular lesions, hair removal, wrinkles, skin tightening, stretch marks, rosacea, sunspots. **Questions patients commonly ask:** **Is Etherea MX safe for all skin types?** Yes. Etherea MX is suitable for Fitzpatrick skin types I–VI. Treatment parameters are adjusted based on skin type and indication. **How does Etherea’s compact design benefit healthcare professionals?** The lightweight system and plug-and-play handpieces support fast setup, easy maneuverability, and efficient workflow in clinical environments. **What is Etherea MX?** Etherea MX is a multi-technology aesthetic platform that integrates eight laser and light-based systems into a single compact device. **Which technologies are included in Etherea MX?** The DUBIMED page lists IPL, Nd:YAG, Er:YAG, fractional picosecond, and infrared modalities among the integrated systems. **What is Etherea MX used for?** According to the page, it is used for treating pigmentation, vascular concerns, and other aesthetic dermatology procedures. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### Etherea MX **URL:** https://dubaimed.com/products/etherea-mx **Brand:** VYDENCE **Product type:** medical_device **Category:** medical-devices **Technical overview:** Etherea MX is a multi-application aesthetic laser platform developed by Vydence Medical (formerly Loktal Medical Electronics, based in Brazil) designed to deliver a comprehensive range of dermatological and aesthetic treatments from a single system. The platform supports multiple interchangeable handpieces and laser/light technologies, including fractional non-ablative laser, fractional ablative laser, long-pulsed Nd:YAG, and intense pulsed light (IPL), making it one of the most versatile multi-platform systems available for aesthetic clinics. Etherea MX addresses a broad spectrum of skin conditions including photoaging, pigmentary disorders such as melasma and sunspots, vascular lesions including spider veins and rosacea, active acne and acne scarring, skin laxity, fine lines and wrinkles, stretch marks, and unwanted hair. The system's modular architecture allows practitioners to combine technologies within a single session for enhanced clinical outcomes through synergistic treatment approaches. Each handpiece is optimized for specific wavelengths and delivery modes, enabling precise energy targeting at different chromophores and tissue depths for safe and effective treatments across all skin types. **Unique features:** Etherea MX stands out as a true multi-platform system that consolidates multiple laser and light technologies into a single compact unit, including fractional non-ablative, fractional ablative, long-pulsed Nd:YAG 1064nm, and IPL capabilities. The platform's modular handpiece system allows clinics to start with core technologies and expand as needed, providing a scalable investment path. Each handpiece features optimized spot sizes, pulse durations, and fluence ranges calibrated for specific clinical indications. The fractional technology offers both ablative and non-ablative modes, enabling practitioners to customize treatment aggressiveness based on patient skin type, condition severity, and acceptable downtime. The Nd:YAG 1064nm handpiece provides deep-penetrating energy suitable for vascular treatments, hair removal on darker skin types, and deep dermal heating for skin tightening. The system's integrated cooling technology protects the epidermis during treatment while maximizing energy delivery to target structures. Etherea MX is designed for safe use across Fitzpatrick skin types I through VI. **Clinical indications:** - skin rejuvenation - pigmentation - laser procedures - melasma - acne scars - vascular lesions - hair removal - wrinkles - skin tightening - stretch marks - rosacea - sunspots **Positioning:** Compared against: laser platform. **Clinician FAQs:** **How often should I receive Etherea treatments** Treatment frequency depends on indication. Most protocols recommend 3–6 sessions spaced 2–4 weeks apart, followed by maintenance. **What is SmartLASER technology and how does it benefit patients?** SmartLASER enables real-time system monitoring, remote diagnostics, and skin-type matched treatment protocols. Enhances safety and treatment precision. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### Etherea MX **Brand:** VYDENCE **Type:** medical_device **Portfolio status:** direct portfolio Universal laser and light-based platform **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. ## Product: SuneKOS – Brand Overview **Brand:** SuneKOS ### For patients ### SuneKOS – Brand Overview ## What is Sunekos? **What it treats:** skin aging, collagen loss, elastin loss, ECM regeneration, skin laxity, fine lines, wrinkles, dehydrated skin, stretch marks, cellulite, skin quality improvement, bio-revitalization, skin firmness, skin elasticity, hair and nail support. **Questions patients commonly ask:** **What is Sunekos and how does it work?** Sunekos is an injectable treatment containing a patented formula of Hyaluronic Acid and 6 Amino Acids (HY6AA PLAAT FORM). It regenerates the Extra Cellular Matrix (ECM) by stimulating fibroblasts in the skin to produce both Collagen and Elastin simultaneously. Unlike standard fillers that physically add volume, Sunekos works biologically — restoring the dermis's own structural proteins from within. **What products are in the Sunekos family?** The Sunekos range includes: Sunekos 1200 (high molecular weight HA scaffold for severe sagging), Sunekos Performa (enhanced pre-mixed bio-revitalizer, Safety in Beauty Global Winner 2022), Sunekos Body (body-specific formula for stretch marks and skin laxity), Sunekos Cell 15 (cellulite treatment with alkaline salts for all 4 stages), and NutraKOS Drinkable (oral amino acid supplement for skin, hair and nails). **Is Sunekos suitable for young patients?** Yes. For younger patients, Sunekos acts as a preventative treatment to slow the physiological aging process. For mature skin, it reactivates cellular functionality and reduces visible signs of aging. It is suitable for both young and mature patients depending on the specific product and indication. **Is there downtime after Sunekos treatment?** No. Sunekos procedures have no downtime and patients can immediately resume their normal activities after treatment. **How long do Sunekos results last?** Results typically last up to 6 months before the treatment cycle needs to be repeated, depending on the patient's skin condition, age, and the specific product used. Most protocols recommend repeating the full cycle twice a year. **When will I see improvements after starting Sunekos?** It is common to see noticeable improvements after the first session. Sunekos acts physiologically, with cumulative results building across the treatment cycle. Some patients report visible hydration and skin quality improvement within days of the first injection. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### SuneKOS – Brand Overview **Brand:** SuneKOS **Product type:** brand_soft_product **Technical overview:** ## What is Sunekos? Sunekos is a clinically proven injectable treatment line developed by Professional Dietetics SpA (Milan, Italy). It uses a patented combination of Hyaluronic Acid (HA) and 6 specific Amino Acids — the HY6AA PLAAT FORM formula — to stimulate fibroblasts in the dermis to produce both Elastin and Collagen simultaneously. This makes Sunekos unique: it regenerates the Extra Cellular Matrix (ECM) from within rather than simply filling or masking the signs of aging. All Sunekos injectable products are registered as CE Medical Device Class III (CE 0373), manufactured in Italy, and distributed exclusively in the Middle East by DubiMed® Medical Supplies Trading. --- ## The Science: HY6AA PLAAT FORM Formula The patented PLAAT FORM formula (International Patent Application PCT/IB2015) identifies the precise composition of Hyaluronic Acid and Amino Acids needed to simultaneously synthesise both Elastin and Collagen: - **Hyaluronic Acid** – Main connective tissue component - **Glycine, L-Proline, L-Lysine** – Collagen Amino Acids - **L-Alanine, L-Valine** – Elastin Amino Acids - **L-Leucine** – Prosynthetic Amino Acid --- ## Sunekos Product Family | Product | Type | Target Area | Key Indication | |---|---|---|---| | Sunekos 1200 | Injectable | Face / Neck | Scaffold for severe sagging | | Sunekos Performa | Injectable | Face / Neck / Hands | Enhanced ECM bio-revitalization | | Sunekos Body | Injectable | Body | Stretch marks & skin laxity | | Sunekos Cell 15 | Injectable | Body | Cellulite (all 4 stages) | | NutraKOS Drinkable | Oral Supplement | Systemic | Skin, hair & nail nutritional support | --- ## Awards & Recognition - Safety in Beauty Diamond Awards 2019 – Winner - Safety in Beauty Diamond Awards 2022 – Innovation & Pioneering Award (European & Global Winner) - Perla Dermatologii Estetycznej 2019 - Cyprus Wellness Awards 2020 **Unique features:** The only injectable brand with the patented HY6AA PLAAT FORM formula that simultaneously produces Elastin AND Collagen. Full body coverage: face, body, cellulite, stretch marks. CE Class III. No downtime. Made in Italy. DubiMed is the exclusive Middle East distributor. **Clinical indications:** - skin aging - collagen loss - elastin loss - ECM regeneration - skin laxity - fine lines - wrinkles - dehydrated skin - stretch marks - cellulite - skin quality improvement - bio-revitalization - skin firmness - skin elasticity - hair and nail support **Clinician FAQs:** **What makes Sunekos different from regular fillers or skin boosters?** Sunekos is the only injectable with the patented HY6AA PLAAT FORM formula — the only proven combination that simultaneously drives both Collagen and Elastin synthesis. Regular fillers add volume temporarily with no regenerative effect. Standard skin boosters hydrate but do not produce structural proteins. Sunekos actually rebuilds the dermis from within. **How long do Sunekos results last?** Results typically last up to 6 months before the treatment cycle needs to be repeated, depending on the patient's skin condition, age, and the specific product used. Most protocols recommend repeating the full cycle twice a year. **What regulatory status do Sunekos injectable products hold?** All Sunekos injectable products are registered as CE Medical Device Class III (CE 0373), manufactured in Italy by Professional Dietetics SpA under strict quality standards. NutraKOS Drinkable is a food supplement subject to food safety regulations. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### SuneKOS – Brand Overview **Brand:** SuneKOS **Type:** brand_soft_product **Portfolio status:** direct portfolio ## What is Sunekos? **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **Who is the exclusive Sunekos distributor in the Middle East?** DubiMed® Medical Supplies Trading is the exclusive Middle East sole distributor for the full Sunekos product line, including all injectable variants and NutraKOS Drinkable. _Note: listed in the internal KB only — no public product page._ ## Product: DUBIMED — Medical Supplies Trading **Brand:** DUBIMED ### For patients ### DUBIMED — Medical Supplies Trading DUBIMED (Dubai Medical Supplies Trading) is the UAE-based Middle East sole distributor and strategic partner for the world's leading aesthetic medical device and cosmeceutical brands. Operating from Dubai, DUBIMED serves aesthetic clinics, dermatology centers, plastic surgery practices, and medical spas across the UAE, GCC, and broader Middle East with a comprehensive portfolio spanning medical devices, soft products (injectables and professional skincare), and full clinical support services. **What it treats:** aesthetic device distribution, cosmeceutical supply, clinical training aesthetic, device maintenance UAE, GCC distribution medical, marketing support clinic, sole distributor Middle East, aesthetic brand partnership. **Regulatory status:** FDA-cleared. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### DUBIMED — Medical Supplies Trading **Brand:** DUBIMED **Product type:** company **Technical overview:** DUBIMED (Dubai Medical Supplies Trading) is the UAE-based Middle East sole distributor and strategic partner for the world's leading aesthetic medical device and cosmeceutical brands. Operating from Dubai, DUBIMED serves aesthetic clinics, dermatology centers, plastic surgery practices, and medical spas across the UAE, GCC, and broader Middle East with a comprehensive portfolio spanning medical devices, soft products (injectables and professional skincare), and full clinical support services. DUBIMED's mission is to elevate the standard of aesthetic medicine in the region by providing clinicians with access to the most clinically proven, technologically advanced products — backed by hands-on training, certified technical support, and dedicated marketing partnerships. ───────────────────────────── MEDICAL DEVICES PORTFOLIO ───────────────────────────── CLASSYS (Korea) — Full Line Distributor: • Ultraformer MPT — MMFU + MPT technology, non-invasive face and body lifting • Volnewmer — 6.78 MHz Monopolar RF skin tightening • Secret Duo — Dual platform: 1540nm Fractional Laser + Microneedle Bipolar RF • Fraxis Duo — Fractional CO2 laser + RF microneedling combination • CuRAS Hybrid — Hybrid aesthetic platform • Secret RF — RF microneedling • Pento — Multi-technology aesthetic platform • Ultraformer III — HIFU face and body lifting (predecessor to MPT) • AquaPure II — Aqua facial + skin care system SOFWAVE (Israel/USA): • Sofwave™ — SUPERB™ 7-beam 1.5mm mid-dermis ultrasound skin tightening CYTRELLIS (USA): • Ellacor® — Micro-coring skin removal device for facial skin laxity VYDENCE (Brazil): • Etherea MX — Multi-technology platform (IPL, Nd:YAG, fractional, RF) • ZYE — Aesthetic energy device SINCLAIR (UK): • Viora V Series — Multi-technology aesthetic platform (RF, IPL, ultrasound) REVANCE (USA): • SkinPen® — FDA-cleared professional microneedling device ───────────────────────────── SOFT PRODUCTS PORTFOLIO ───────────────────────────── MESOESTETIC® (Spain) — Full Line Distributor: • mesohyal® — Injectable mesotherapy hyaluronic acid line • cosmelan® — Professional depigmentation treatment system • dermamelan® — Advanced professional depigmentation method • dermamelan® intimate — Intimate area depigmentation • traneX glow — Tranexamic acid brightening treatment • blemiderm® — Anti-blemish professional treatment ANTEAGE® (USA / Cellese Biological Lab) — Middle East Sole Distributor: • AnteAGE® MDX Biosome™ — Biomimetic exosome treatment (Skin, Brightening, Hair) • AnteAGE® MDX Exosome — Real Bone Marrow Stem Cell exosomes • AnteAGE® MD — Professional in-clinic growth factor microneedling systems • AnteAGE® MD Home Care — Daily maintenance growth factor home system SUNEKOS (Italy) — Middle East Distributor: • SuneKOS — Injectable amino acid + hyaluronic acid biostimulator for skin regeneration CELLENIS® — Middle East Distributor: • Cellenis® PRP — Professional platelet-rich plasma system for skin and hair ───────────────────────────── SERVICES ───────────────────────────── 1. BIOMEDICAL SERVICE: Certified maintenance and technical support for all medical devices in the DUBIMED portfolio. Factory-trained engineers ensure devices perform at peak specification with minimal downtime. 2. CLINICAL TRAINING: Hands-on training and workshops for aesthetic practitioners. Protocol-based training for every device and product in the portfolio — from beginner onboarding to advanced technique workshops. Delivered by certified clinical educators. 3. LOGISTICS & DISTRIBUTION: Reliable delivery network across the GCC. Cold-chain capable for temperature-sensitive products (exosomes, biologics). Covers UAE, Saudi Arabia, Qatar, Bahrain, Oman, Kuwait. 4. MARKETING SUPPORT: Marketing strategies and digital campaigns tailored for aesthetic clinics. Includes co-branded social content, patient education materials, before/after documentation support, and clinic digital presence enhancement. **Unique features:** DUBIMED COMPETITIVE ADVANTAGES: 1. WIDEST AESTHETIC PORTFOLIO IN THE MIDDLE EAST: DUBIMED is the only distributor in the Middle East simultaneously holding sole distribution rights for CLASSYS (Korea), AnteAGE (USA), and key brands from Sofwave, Cytrellis, Vydence, Sinclair, Revance, Mesoestetic, Sunekos, and Cellenis — giving clinics a single, trusted source for their entire device and consumable needs. 2. DEVICE + CONSUMABLE SYNERGY: DUBIMED uniquely pairs best-in-class devices with the best consumables designed to work with them. Examples: - Secret Duo (RF microneedling) + AnteAGE MDX Exosome/Biosome (post-treatment recovery and amplification) - Ultraformer MPT (HIFU) + SuneKOS (skin biostimulation) - SkinPen (microneedling) + AnteAGE MD Microneedling Solution This integrated approach allows clinics to offer complete treatment protocols — not just individual devices. 3. FULL-SERVICE DISTRIBUTOR (not just sales): Four service pillars support every clinic in the portfolio: - Biomedical Service: certified technical support and maintenance - Clinical Training: hands-on workshops and protocol training - Logistics & Distribution: GCC-wide cold chain and delivery - Marketing Support: clinic campaigns, patient education, digital content 4. GCC-WIDE REACH: Distribution and logistics network covering UAE, Saudi Arabia, Qatar, Bahrain, Oman, and Kuwait — ensuring fast delivery and service response times throughout the region. 5. EXCLUSIVE MIDDLE EAST PARTNERSHIPS: Direct, exclusive distribution agreements with manufacturers ensure DUBIMED clients receive authentic products at best prices, with manufacturer-backed training and support — not through grey market or secondary channels. **Clinical indications:** - aesthetic device distribution - cosmeceutical supply - clinical training aesthetic - device maintenance UAE - GCC distribution medical - marketing support clinic - sole distributor Middle East - aesthetic brand partnership **Regulatory status:** - FDA-cleared **Positioning:** Also known as: DUBIMED, DubiMed, Dubai Medical Supplies Trading, Dubi Med, dubaimed.com, DUBIMED UAE, دوبيميد, دوبي ميد, تجارة المستلزمات الطبية دبي. Compared against: Medline, Healthmark, Gulf Medical, Derma Gulf, Aesthetic Solutions, Innoaesthetics distributor, Allergan distributor UAE, Galderma UAE, Sinclair Pharma UAE, other aesthetic distributors GCC. **Clinician FAQs:** **What is DUBIMED and what does it do?** DUBIMED (Dubai Medical Supplies Trading) is a UAE-based company specializing in the distribution of premium aesthetic medical devices and professional skincare (soft products) across the Middle East and GCC. DUBIMED serves as the official Middle East sole distributor for several globally recognized brands, supplying aesthetic clinics, dermatology centers, plastic surgery practices, and medical spas with: - Medical devices: energy-based and non-energy-based aesthetic platforms - Soft products: professional injectables, cosmeceuticals, exosome treatments, and home care systems - Clinical services: training, biomedical support, logistics, and marketing DUBIMED operates from Dubai and distributes across the UAE, Saudi Arabia, Qatar, Bahrain, Oman, and Kuwait. **What medical devices does DUBIMED distribute?** DUBIMED distributes medical devices from six leading international manufacturers: CLASSYS (South Korea) — Full portfolio: - Ultraformer MPT: MMFU + Micro-focused Pulse Technology, non-invasive face/body lifting - Volnewmer: 6.78 MHz Monopolar RF skin tightening (4 treatment tips) - Secret Duo: Dual platform — 1540nm Fractional Laser + Microneedle Bipolar RF - Fraxis Duo: Fractional CO2 laser + RF microneedling - CuRAS Hybrid: Hybrid multi-technology aesthetic platform - Secret RF: RF microneedling - Pento: Multi-technology platform - Ultraformer III: HIFU face and body lifting - AquaPure II: Aqua facial and skin care system SOFWAVE (Israel/USA): - Sofwave™: SUPERB™ 7-parallel-beam ultrasound, targets 1.5mm mid-dermis CYTRELLIS (USA): - Ellacor®: Micro-coring device — removes micro-columns of skin tissue for facial laxity VYDENCE (Brazil): - Etherea MX: Multi-technology platform (IPL, Nd:YAG, fractional, RF) - ZYE: Aesthetic energy device SINCLAIR (UK): - Viora V Series: Multi-technology aesthetic platform (RF, IPL, ultrasound) REVANCE (USA): - SkinPen®: FDA-cleared professional microneedling device **What soft products and skincare brands does DUBIMED distribute?** DUBIMED distributes professional soft products from four leading brands: MESOESTETIC® (Spain) — Full line distributor: - mesohyal®: Injectable mesotherapy hyaluronic acid line for skin hydration and biorevitalization - cosmelan®: The world's leading professional depigmentation treatment - dermamelan®: Advanced professional depigmentation method for resistant melasma - dermamelan® intimate: Intimate area depigmentation system - traneX glow: Tranexamic acid professional brightening treatment - blemiderm®: Anti-blemish and acne professional treatment system ANTEAGE® (USA — Cellese Biological Lab) — Middle East Sole Distributor: - AnteAGE® MDX Biosome™: Biomimetic exosome treatment. 25 Billion Biosomes. Skin, Brightening, Hair formulations. FDA MoCRA registered. Room temperature stable. - AnteAGE® MDX Exosome: Real Bone Marrow Stem Cell exosomes. 5 Billion real exosomes. 6,000 growth factors. The only BMSC exosome in the world. - AnteAGE® MD: Professional in-clinic growth factor microneedling solutions (Skin, Brightening, Hair) - AnteAGE® MD Home Care: Daily maintenance home system (Serum, Accelerator, Brightener, Hair SCS, Hair Polybotanical) SUNEKOS (Italy) — Middle East Distributor: - SuneKOS: Injectable biostimulator combining amino acids + hyaluronic acid for dermal regeneration CELLENIS® — Middle East Distributor: - Cellenis® PRP: Professional platelet-rich plasma preparation system for skin and hair treatments **What services does DUBIMED offer to clinics and partners?** Beyond product supply, DUBIMED provides four core service pillars to support every clinic in its network: 1. BIOMEDICAL SERVICE: Certified maintenance and technical support for all devices in the DUBIMED portfolio. Factory-trained biomedical engineers perform preventive maintenance, calibration, repairs, and emergency support. Ensures maximum device uptime and performance consistency for clinics. 2. CLINICAL TRAINING: Hands-on training and workshops for doctors, nurses, and aesthetic practitioners. Covers: - Device operation and treatment protocols - Clinical indications and patient selection - Combination treatment strategies - Live patient demonstration sessions Training is product- and protocol-specific, delivered by certified clinical educators at DUBIMED facilities or at clinic premises. 3. LOGISTICS & DISTRIBUTION: Reliable delivery network across the entire GCC region including UAE, Saudi Arabia, Qatar, Bahrain, Oman, and Kuwait. Cold-chain logistics capability for temperature-sensitive biologics (exosomes, PRP systems). Inventory management and fast replenishment service for consumables. 4. MARKETING SUPPORT: Strategic marketing assistance tailored for aesthetic clinics: - Co-branded social media content and campaigns - Patient education materials (brochures, digital assets) - Before/after documentation and case study support - Digital presence and clinic profile enhancement - Product launch support and promotional campaigns **Which countries does DUBIMED cover?** DUBIMED distributes across the GCC (Gulf Cooperation Council) and broader Middle East region, covering: - UAE (United Arab Emirates) — Primary market and headquarters - Saudi Arabia (KSA) - Qatar - Bahrain - Oman - Kuwait For several brands, DUBIMED holds the title of "Middle East Sole Distributor" — meaning they are the only authorized source for those brands across the entire Middle East region, not just the GCC. This applies to brands including AnteAGE® and Secret DUO (ilooda). Clinics in any of these territories can contact DUBIMED for product orders, clinical training, device demonstrations, and biomedical service. **How can a clinic become a DUBIMED partner or place an order?** To become a DUBIMED partner or place an order, clinics and practitioners can reach out through the following channels: Website: www.dubaimed.com Instagram: @dubimed YouTube: DUBIMED channel Facebook: DUBIMED page Through the website, clinics can: - Browse the full product and device portfolio - Submit a contact or enquiry form - Request a product demonstration - Enquire about training and workshops - Request biomedical service DUBIMED works with licensed aesthetic clinics, dermatology practices, plastic surgery centers, and medical spas across the UAE and GCC. All sales are B2B (business to business) — products are supplied to healthcare professionals and licensed clinics only, not directly to end consumers. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### DUBIMED — Medical Supplies Trading **Brand:** DUBIMED **Type:** company **Portfolio status:** direct portfolio DUBIMED (Dubai Medical Supplies Trading) is the UAE-based Middle East sole distributor and strategic partner for the world's leading aesthetic medical device and cosmeceutical brands. Operating from Dubai, DUBIMED serves aesthetic clinics, dermatology centers, plastic surgery practices, and medical spas across the UAE, GCC, and broader Middle East with a comprehensive portfolio spanning medical devices, soft products (injectables and professional skincare), and full clinical support services. **Market access:** FDA-cleared. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **What is DUBIMED and what does it do?** DUBIMED (Dubai Medical Supplies Trading) is a UAE-based company specializing in the distribution of premium aesthetic medical devices and professional skincare (soft products) across the Middle East and GCC. DUBIMED serves as the official Middle East sole distributor for several globally recognized brands, supplying aesthetic clinics, dermatology centers, plastic surgery practices, and medical spas with: - Medical devices: energy-based and non-energy-based aesthetic platforms - Soft products: professional injectables, cosmeceuticals, exosome treatments, and home care systems - Clinical services: training, biomedical support, logistics, and marketing DUBIMED operates from Dubai and distributes across the UAE, Saudi Arabia, Qatar, Bahrain, Oman, and Kuwait. **What medical devices does DUBIMED distribute?** DUBIMED distributes medical devices from six leading international manufacturers: CLASSYS (South Korea) — Full portfolio: - Ultraformer MPT: MMFU + Micro-focused Pulse Technology, non-invasive face/body lifting - Volnewmer: 6.78 MHz Monopolar RF skin tightening (4 treatment tips) - Secret Duo: Dual platform — 1540nm Fractional Laser + Microneedle Bipolar RF - Fraxis Duo: Fractional CO2 laser + RF microneedling - CuRAS Hybrid: Hybrid multi-technology aesthetic platform - Secret RF: RF microneedling - Pento: Multi-technology platform - Ultraformer III: HIFU face and body lifting - AquaPure II: Aqua facial and skin care system SOFWAVE (Israel/USA): - Sofwave™: SUPERB™ 7-parallel-beam ultrasound, targets 1.5mm mid-dermis CYTRELLIS (USA): - Ellacor®: Micro-coring device — removes micro-columns of skin tissue for facial laxity VYDENCE (Brazil): - Etherea MX: Multi-technology platform (IPL, Nd:YAG, fractional, RF) - ZYE: Aesthetic energy device SINCLAIR (UK): - Viora V Series: Multi-technology aesthetic platform (RF, IPL, ultrasound) REVANCE (USA): - SkinPen®: FDA-cleared professional microneedling device **What soft products and skincare brands does DUBIMED distribute?** DUBIMED distributes professional soft products from four leading brands: MESOESTETIC® (Spain) — Full line distributor: - mesohyal®: Injectable mesotherapy hyaluronic acid line for skin hydration and biorevitalization - cosmelan®: The world's leading professional depigmentation treatment - dermamelan®: Advanced professional depigmentation method for resistant melasma - dermamelan® intimate: Intimate area depigmentation system - traneX glow: Tranexamic acid professional brightening treatment - blemiderm®: Anti-blemish and acne professional treatment system ANTEAGE® (USA — Cellese Biological Lab) — Middle East Sole Distributor: - AnteAGE® MDX Biosome™: Biomimetic exosome treatment. 25 Billion Biosomes. Skin, Brightening, Hair formulations. FDA MoCRA registered. Room temperature stable. - AnteAGE® MDX Exosome: Real Bone Marrow Stem Cell exosomes. 5 Billion real exosomes. 6,000 growth factors. The only BMSC exosome in the world. - AnteAGE® MD: Professional in-clinic growth factor microneedling solutions (Skin, Brightening, Hair) - AnteAGE® MD Home Care: Daily maintenance home system (Serum, Accelerator, Brightener, Hair SCS, Hair Polybotanical) SUNEKOS (Italy) — Middle East Distributor: - SuneKOS: Injectable biostimulator combining amino acids + hyaluronic acid for dermal regeneration CELLENIS® — Middle East Distributor: - Cellenis® PRP: Professional platelet-rich plasma preparation system for skin and hair treatments **What services does DUBIMED offer to clinics and partners?** Beyond product supply, DUBIMED provides four core service pillars to support every clinic in its network: 1. BIOMEDICAL SERVICE: Certified maintenance and technical support for all devices in the DUBIMED portfolio. Factory-trained biomedical engineers perform preventive maintenance, calibration, repairs, and emergency support. Ensures maximum device uptime and performance consistency for clinics. 2. CLINICAL TRAINING: Hands-on training and workshops for doctors, nurses, and aesthetic practitioners. Covers: - Device operation and treatment protocols - Clinical indications and patient selection - Combination treatment strategies - Live patient demonstration sessions Training is product- and protocol-specific, delivered by certified clinical educators at DUBIMED facilities or at clinic premises. 3. LOGISTICS & DISTRIBUTION: Reliable delivery network across the entire GCC region including UAE, Saudi Arabia, Qatar, Bahrain, Oman, and Kuwait. Cold-chain logistics capability for temperature-sensitive biologics (exosomes, PRP systems). Inventory management and fast replenishment service for consumables. 4. MARKETING SUPPORT: Strategic marketing assistance tailored for aesthetic clinics: - Co-branded social media content and campaigns - Patient education materials (brochures, digital assets) - Before/after documentation and case study support - Digital presence and clinic profile enhancement - Product launch support and promotional campaigns **Which countries does DUBIMED cover?** DUBIMED distributes across the GCC (Gulf Cooperation Council) and broader Middle East region, covering: - UAE (United Arab Emirates) — Primary market and headquarters - Saudi Arabia (KSA) - Qatar - Bahrain - Oman - Kuwait For several brands, DUBIMED holds the title of "Middle East Sole Distributor" — meaning they are the only authorized source for those brands across the entire Middle East region, not just the GCC. This applies to brands including AnteAGE® and Secret DUO (ilooda). Clinics in any of these territories can contact DUBIMED for product orders, clinical training, device demonstrations, and biomedical service. **How can a clinic become a DUBIMED partner or place an order?** To become a DUBIMED partner or place an order, clinics and practitioners can reach out through the following channels: Website: www.dubaimed.com Instagram: @dubimed YouTube: DUBIMED channel Facebook: DUBIMED page Through the website, clinics can: - Browse the full product and device portfolio - Submit a contact or enquiry form - Request a product demonstration - Enquire about training and workshops - Request biomedical service DUBIMED works with licensed aesthetic clinics, dermatology practices, plastic surgery centers, and medical spas across the UAE and GCC. All sales are B2B (business to business) — products are supplied to healthcare professionals and licensed clinics only, not directly to end consumers. _Note: listed in the internal KB only — no public product page._ ## Product: SuneKOS 1200 **Brand:** SuneKOS ### For patients ### SuneKOS 1200 ## What is Sunekos 1200? **What it treats:** severe sagging, deep wrinkles, nasolabial folds, facial volume loss, neck laxity, structural support, crow's feet, skin aging face. **Questions patients commonly ask:** **What needle or cannula is used with Sunekos 1200?** Sunekos 1200 is always administered via a cannula (25-27-30G, 40-50mm) using the Fan Technique, injected into the medium to deep dermis. It is not administered with a fine needle technique. **How does Sunekos 1200 differ from Sunekos 200?** Sunekos 200 uses low molecular weight HA (200 KD) for bio-revitalization in the medium dermis and is used across all treatment sessions. Sunekos 1200 uses high molecular weight HA (1200 KD) as a structural scaffold in the deep dermis and is used only in Session 1. They work synergistically in the Cushion Technique. **What does one pack of Sunekos 1200 contain?** One pack of Sunekos 1200 contains 1 treatment of 3ml: 1x bottle of high molecular weight (1200 KD) Sodium Hyaluronate sterile gel (24mg/1.5ml) and 1x bottle of sterile Amino Acid solution (100mg/1.5ml). **How many times per year should the Cushion Technique cycle be repeated?** The full Cushion Technique cycle — 1 session of Sunekos 1200 followed by 3 sessions of Sunekos Performa or 200 at 14-day intervals — should be repeated 2 times per year. **Which face and body areas does Sunekos 1200 treat?** Sunekos 1200 is indicated for the forehead, full face (particularly nasolabial folds and cheeks), dark eye circles and bags, neck, décolleté, and hands — specifically in patients with severe volume depletion, structural sagging, and deep wrinkles requiring additional scaffold support. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### SuneKOS 1200 **Brand:** SuneKOS **Product type:** soft_product **Technical overview:** ## What is Sunekos 1200? Sunekos 1200 is a high molecular weight (1200 KD) injectable Sodium Hyaluronate gel combined with a sterile Amino Acid solution, used as a **deep dermal scaffold** to provide structural support in the treatment of severe skin sagging and deep wrinkles. Registered as CE Medical Device Class III, manufactured in Italy. --- ## Composition - **1x bottle (HA):** High molecular weight (1200 KD) Sodium Hyaluronate sterile gel — 24mg / 1.5ml - **1x bottle (AA):** Sterile Amino Acid solution — 100mg / 1.5ml - **One pack contains:** 1 treatment of 3ml --- ## How It Works Sunekos 1200 uses the patented HY6AA PLAAT FORM formula. Its high molecular weight HA provides a physical scaffold in the deep dermis while the 6 Amino Acids stimulate fibroblasts to produce new Elastin and Collagen — restoring both the biological function of the dermis and the naturally youthful appearance of the skin. --- ## Treatment Areas Forehead | Full Face | Dark Eye Circles & Bags | Neck | Décolleté | Hands --- ## Injection Technique — Cushion Technique (Session 1 only) Indicated for: **severe wrinkles & sagging skin** **Sunekos 1200 — scaffold layer:** - Cannula 25-27-30G, 40-50mm - Fan Technique - Medium / Deep Dermis - Used only in Session 1; all subsequent sessions use Sunekos Performa or 200 **Full Protocol:** | Session | Product | Timing | |---|---|---| | 1 | Sunekos 1200 + Sunekos Performa/200 (same day) | Day 0 | | 2 | Sunekos Performa or 200 | +14 days | | 3 | Sunekos Performa or 200 | +14 days | | 4 (optional) | Sunekos Performa or 200 | +14 days | Repeat the full cycle **2 times per year**. --- ## Clinical Evidence Internal trial comparing Sunekos 200 alone vs Sunekos 1200 + Sunekos 200 (Cushion Technique): - **+24%** improvement in Facial Volume Measurement - **+33%** improvement in FVLS photographic scale **Unique features:** High molecular weight (1200 KD) HA deep scaffold — used exclusively as the Session 1 foundation in the Cushion Technique. Clinically proven +24% facial volume and +33% FVLS improvement vs Sunekos 200 alone. CE Class III. 1 treatment per pack (3ml). **Clinical indications:** - severe sagging - deep wrinkles - nasolabial folds - facial volume loss - neck laxity - structural support - crow's feet - skin aging face **Positioning:** Also known as: sunekos 1200, S1200, cushion technique sunekos, scaffold filler sunekos. Compared against: Profhilo, Juvederm Voluma, Sculptra, Radiesse, Teosyal Ultimate, Ellanse. **Clinician FAQs:** **What is Sunekos 1200 used for?** Sunekos 1200 is used as a deep structural scaffold for patients with severe skin sagging, deep nasolabial folds, and significant facial volume loss. It is always used in combination with Sunekos 200 or Sunekos Performa as part of the Cushion Technique protocol — never as a standalone treatment. **What is the Cushion Technique and why is Sunekos 1200 needed for it?** The Cushion Technique is a combined protocol for severe wrinkles and sagging skin. Sunekos 1200 is injected first — on the same day as the first Sunekos Performa or 200 session — using a cannula into the deep dermis, creating a high molecular weight HA structural scaffold. This base is then progressively built upon by the bio-regenerative action of subsequent Sunekos Performa or 200 sessions. The combination demonstrated +24% facial volume improvement and +33% FVLS photographic scale improvement over Sunekos 200 alone. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### SuneKOS 1200 **Brand:** SuneKOS **Type:** soft_product **Portfolio status:** direct portfolio ## What is Sunekos 1200? **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **Can Sunekos 1200 be used alone?** No. Sunekos 1200 is designed exclusively as a first-session scaffold within the Cushion Technique. It must always be followed by Sunekos Performa or Sunekos 200 in subsequent sessions. Using it alone does not deliver the full therapeutic benefit. _Note: listed in the internal KB only — no public product page._ ## Product: SuneKOS Performa **Brand:** SuneKOS ### For patients ### SuneKOS Performa ## What is SuneKOS Performa? **What it treats:** anti-aging, wrinkles, skin laxity, skin compactness, photoaging, dark circles, deep hydration, facial volume loss, skin texture, dyschromia, skin renovation, lifting, volumizing. **Questions patients commonly ask:** **How does SuneKOS Performa protect hyaluronic acid from enzymatic degradation?** Through two physical mechanisms: first, the hydrophobic properties of the 6AA formula create a physical shield around HA molecules; second, L-Lysine (a strongly positively charged amino acid) contrasts the negative electrical charge of HA, reducing hyaluronidase binding. Together these reduce hyaluronidase-mediated HA degradation by 40%, extending the duration and effectiveness of the treatment. **What injection techniques are used with SuneKOS Performa?** Three main techniques: IFT (Interstitial Fluid Technique) for lifting in young/round-faced patients — injections follow interstitial fluid flow at 45° with massage in the flow direction. RIFT (Reverse Interstitial Fluid Technique) for volumizing in thin/elongated-faced patients — injections and massage go against the flow for an immediate volumizing effect. Cushion Technique — combined with SuneKOS 1200 on Session 1 for severe sagging. **What does one pack of SuneKOS Performa contain?** One pack of SuneKOS Performa contains 2 treatments of 3.5ml each, pre-mixed: 2x sterile vials of Hyaluronic Acid (200 KD) at 35mg/3.5ml with lyophilised Amino Acids at 128mg/3.5ml. **What clinical results has SuneKOS Performa demonstrated?** A study on 10 patients demonstrated +50% improvement in skin compactness and -49% reduction in photoageing dyschromia. When used in the Cushion Technique with SuneKOS 1200, clinical results showed significant facial volume restoration and wrinkle reduction maintained up to 6 months. **When will patients see results with SuneKOS Performa?** Noticeable improvements are commonly seen after the first session. SuneKOS Performa acts physiologically, with cumulative results building across the treatment cycle. Measurable skin compactness improvements and reduction in photoageing signs are observable from the early stages of the treatment programme. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### SuneKOS Performa **Brand:** SuneKOS **Product type:** soft_product **Technical overview:** ## What is SuneKOS Performa? SuneKOS Performa is the latest and most advanced evolution of the SuneKOS injectable line — the enhanced formula for skin renovation. It combines low molecular weight Hyaluronic Acid (200 KD) with a significantly higher concentration of Amino Acids in a new AA vs HA ratio, presented as a **ready pre-mixed solution** — no reconstitution required at treatment time. Winner: **Safety in Beauty Diamond Awards 2022 — Innovation & Pioneering Award, European & Global Winner**. --- ## Composition - **2x sterile vials of Hyaluronic Acid (200 KD):** 35mg / 3.5ml - **Ready mix with lyophilised Amino Acids:** 128mg / 3.5ml (pre-mixed — no preparation needed) - **One pack contains:** 2 treatments of 3.5ml each --- ## Key Innovations Over SuneKOS 200 **1. Hyaluronidase Protection (-40%)** The higher AA concentration physically protects HA from enzymatic degradation by reducing hyaluronidase activity by **40%**, achieved through two mechanisms: - The hydrophobic properties of the 6AA formula physically shield HA molecules - L-Lysine (strongly positively charged) contrasts the negative electrical charge of HA, reducing hyaluronidase binding Result: increased HA presence at the injection site → **prolonged duration of action**. **2. Full Collagen Spectrum** Performa promotes production of Elastin and all main types of reticular collagen fibres, including **Type IV and Type VII** (anchoring fibres and plaques) — a more complete ECM reconstruction than SuneKOS 200. --- ## Clinical Study Results (10 patients) - **+50%** improvement in Skin Compactness - **-49%** reduction in Photoageing Dyschromia --- ## Treatment Areas Forehead | Full Face | Dark Eye Circles & Bags | Neck | Décolleté | Hands --- ## Injection Techniques **IFT — Interstitial Fluid Technique** *(Lifting — young, round-faced patients)* - Needle 27-30G, 12-13mm | 45° inclination | Medium-deep dermis - 0.1ml per point at ~1.5cm distance | Massage following the flow direction - Protocol: 4 sessions × every 7-10 days | Repeat 2x/year **RIFT — Reverse Interstitial Fluid Technique** *(Volumizing — thin/elongated-faced patients)* - Same needle/cannula specs | Injections sequence against the flow - Massage against the flow for immediate volumizing effect - Protocol: 4 sessions × every 7-10 days | Repeat 2x/year **HPT — High Performance Technique** *(Full Face with Performa alone)* - Needle 30-32G (4-13mm) or Cannula 25-27-30G (40-50mm) - 1ml syringe recommended | Medium/deep dermis | 0.1ml per point - 1 session every 2 weeks × 3 sessions (optional 4th) - Repeat cycle 2x/year **Cushion Technique** *(Severe wrinkles & sagging — combined with SuneKOS 1200)* - Session 1: SuneKOS 1200 + SuneKOS Performa same day - Sessions 2, 3 (+optional 4): SuneKOS Performa only, every 14 days - Repeat cycle 2x/year **Unique features:** Only SuneKOS injectable with ready pre-mixed formula. New AA/HA ratio reduces hyaluronidase degradation by -40% for longer-lasting HA. Produces full collagen spectrum including anchoring Type IV & VII. Safety in Beauty Global Winner 2022. +50% skin compactness. 2 treatments per pack. **Clinical indications:** - anti-aging - wrinkles - skin laxity - skin compactness - photoaging - dark circles - deep hydration - facial volume loss - skin texture - dyschromia - skin renovation - lifting - volumizing **Positioning:** Also known as: SuneKOS Performa, SK Performa, sunekos enhanced, sunekos new formula, performa injectable, sunekos pre-mixed. Compared against: Profhilo, Juvederm Volite, Restylane Skinboosters, Sculptra, Teosyal Redensity, Jalupro, Belotero Revive. **Clinician FAQs:** **What is SuneKOS Performa and how is it different from SuneKOS 200?** SuneKOS Performa is the latest evolution of the SuneKOS injectable line. It has a higher Amino Acid concentration (128mg vs 100mg) and a new AA vs HA ratio that reduces hyaluronidase activity by 40% — keeping HA active longer at the injection site. It also promotes a wider collagen spectrum including anchoring Type IV and Type VII collagen. It comes pre-mixed, requiring no reconstitution. **Is SuneKOS Performa pre-mixed?** Yes. SuneKOS Performa comes already pre-mixed in the vial — no preparation or reconstitution is needed at treatment time. This saves clinical preparation time and ensures precise, consistent dosing with every use. **What is the standard SuneKOS Performa treatment protocol for the full face?** For full face (HPT): needle 30-32G (4-13mm) or cannula 25-27-30G (40-50mm), 0.1ml per point, medium/deep dermis, 1 session every 2 weeks for 3 sessions (optional 4th). Repeat the cycle 2 times per year. For the Cushion Technique with SuneKOS 1200: Session 1 uses both products on the same day; Sessions 2, 3 (and optional 4) use only Performa at 14-day intervals. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### SuneKOS Performa **Brand:** SuneKOS **Type:** soft_product **Portfolio status:** direct portfolio ## What is SuneKOS Performa? **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. _Note: listed in the internal KB only — no public product page._ ## Product: SuneKOS Body **Brand:** SuneKOS ### For patients ### SuneKOS Body ## What is SuneKOS Body? **What it treats:** stretch marks, striae distensae, striae alba, skin laxity body, arms laxity, abdomen laxity, thigh laxity, knee laxity, post-pregnancy skin, body skin aging, body contouring. **Questions patients commonly ask:** **What conditions does SuneKOS Body treat?** SuneKOS Body treats two main conditions: stretch marks (striae distensae and striae alba) in the thighs, abdomen, arms, and knees; and skin laxity in the arms, inner thighs, knees, and abdomen. The HY6AA formula is specifically adapted to the dermal density of each body region. **How many sessions are needed for stretch marks?** A course of 3 to 4 injection sessions administered once every 15 days is recommended for stretch mark treatment. **How is SuneKOS Body used for skin laxity?** Using the ATL (Across Tension Lines) technique, injections are made perpendicularly to the skin tension lines. For arms: 2.5-5ml per arm via cannula (0.3ml/point) or needle (0.1ml/point, 4-6 points per line). For abdomen: 5ml upper + 5ml lower totalling 10ml. For legs/thighs: 5ml per part. A minimum of 3 sessions is recommended for all laxity areas. **What does one pack of SuneKOS Body contain?** One pack of SuneKOS Body contains 1 treatment (10ml reconstituted): 1x vial Sodium Hyaluronate (low density) and 1x bottle Amino Acids solution. **Can SuneKOS Body treat both new and old stretch marks?** Yes. SuneKOS Body is indicated for both striae distensae (newer, often reddish/purple stretch marks with active ECM disruption) and striae alba (older, white/silver stretch marks with established atrophy). The product helps restore the disrupted elastic and collagen fibre architecture back towards a normal dermis structure. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### SuneKOS Body **Brand:** SuneKOS **Product type:** soft_product **Technical overview:** ## What is SuneKOS Body? SuneKOS Body is a 10ml injectable solution containing low density Hyaluronic Acid (HA) combined with Amino Acids (AA) using the HY6AA formula (Glycine, L-Proline, L-Lysine, L-Leucine, L-Valine, L-Alanine) — specifically balanced for the dermis of the body. It promotes production of **Collagen Type IV and Elastin**, rebuilding the Extra Cellular Matrix (ECM) components. Registered as CE Medical Device Class III, manufactured in Italy. The HY6AA PLAAT FORM formula has been specifically adapted to the different dermal density of each body region. --- ## Composition - **1x vial:** Sodium Hyaluronate (low density) - **1x bottle:** Amino Acids solution - **Reconstituted as:** 10ml — 1 treatment per pack --- ## Indications & Treatment Areas ### Stretch Marks (Striae Distensae / Striae Alba) Direct injection into the dermal wall of the stretch mark at three depths — superficial, medium, and deep dermis — to rebuild disrupted elastin and collagen fibres. Target areas: thighs, abdomen, arms, knees. ### Skin Laxity Arms | Abdomen | Inner Thighs | Knees --- ## Injection Techniques ### Stretch Marks — Micro-Bolus Technique - Needle: 30-32G, 12-13mm - Inclination: 30°-40° - Technique: series of 3 micro-boluses at 3 dermal depths (superficial / medium / deep) - Volume: 0.2ml per bolus - Injection site: directly into the wall of the stretch mark - Sessions: 3–4 times, once every 15 days - Example volume: thigh stretch marks → 5ml per side ### Skin Laxity — ATL (Across Tension Lines) Technique | Area | Volume | Cannula | Needle | |---|---|---|---| | Arms | 2.5–5ml per arm | 0.3ml/point, 1-2 areas/arm | 0.1ml/point, 4-6 pts/line | | Abdomen | 5ml upper + 5ml lower (10ml total) | 1ml/point | 0.1ml/point, 10 pts/line | | Legs (Thigh & Gluteus) | 5ml per part | 1ml/point, 10ml/side | 0.1ml/point, 6-10 pts × 10 lines | All areas: minimum **3 sessions**. --- ## Clinical Results (Skin Laxity Study) 21 patients, 4 injections once weekly, using only ½ vial (5ml) per area: - Improvement of at least 1 grade on visual score in inner knee and thigh - Results maintained at T8 (2 months) and T16 (4 months) post first injection **Unique features:** Only SuneKOS product specifically formulated for body dermal density. Dual indication: stretch marks (3-depth micro-bolus directly into the stretch mark wall) and skin laxity (ATL technique). Promotes Collagen Type IV + Elastin. 10ml per treatment. CE Class III. **Clinical indications:** - stretch marks - striae distensae - striae alba - skin laxity body - arms laxity - abdomen laxity - thigh laxity - knee laxity - post-pregnancy skin - body skin aging - body contouring **Positioning:** Also known as: SuneKOS Body, SK Body, sunekos stretch marks, sunekos body laxity. Compared against: Sculptra body, Radiesse body, Lanluma, Ellanse body, Juvederm Voluma body. **Clinician FAQs:** **How is SuneKOS Body injected for stretch marks?** Using a 30-32G needle (12-13mm) at a 30°-40° inclination, a series of 3 micro-boluses of 0.2ml each is injected directly into the wall of the stretch mark at three dermal depths — superficial, medium, and deep. The number of injection points depends on the stretch mark dimension. This is repeated 3-4 times, once every 15 days. For thigh stretch marks, 5ml is used per side. **What makes SuneKOS Body different from the facial SuneKOS products?** All SuneKOS products share the HY6AA PLAAT FORM formula, but SuneKOS Body uses a low-density formulation specifically calibrated for the thicker, differently structured dermis of the body. It also specifically promotes Collagen Type IV production — critical for the basement membrane, the layer most severely disrupted in stretch marks. **What clinical evidence supports SuneKOS Body for skin laxity?** A study of 21 patients injected 4 times weekly, using only half a vial (5ml) per area for arms and legs, showed a clinically meaningful improvement of at least 1 grade reduction on the visual laxity score for the inner knee and thigh. Results were maintained at 2 months and 4 months after the first injection. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### SuneKOS Body **Brand:** SuneKOS **Type:** soft_product **Portfolio status:** direct portfolio ## What is SuneKOS Body? **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. _Note: listed in the internal KB only — no public product page._ ## Product: SuneKOS Cell 15 **Brand:** SuneKOS ### For patients ### SuneKOS Cell 15 ## What is SuneKOS Cell 15? **What it treats:** cellulite, EFP, edematous fibrosclerotic panniculopathy, orange peel skin, skin dimpling, thigh cellulite, gluteal cellulite, body contouring, tissue acidosis, skin fibrosis, microcirculation, body laxity. **Questions patients commonly ask:** **What are the 4 stages of cellulite and how does SuneKOS Cell 15 address each?** Stages I & II present as edemato-inflammatory conditions with hypo-oxygenation and tissue acidosis — treated with the ATL-n needle technique (30G, 12mm, 30° inclination, medium-deep dermis, 0.15ml per point). Stages III & IV involve established fibrosis, sclerosis, and inflamm-aging — treated with the more penetrating ATL-c cannula technique (27G/40-50mm or 22G/50-70mm, deep dermis/upper hypodermis, fan technique, 0.8ml per injection). Both share the same alkaline salt formula to counter acidosis. **Why do the Carbonate/Bicarbonate alkaline salts matter in cellulite treatment?** Tissue acidosis — a chronic reduction in pH in the subcutaneous layers — is a key driver of the inflammation and fibrosis that characterise all stages of cellulite, especially stages III and IV. The alkaline salts in SuneKOS Cell 15 specifically rebalance this acidosis, reduce ECM inflammation to counter fibrosis progression, and help restore physiological pH. No other cellulite injectable currently addresses this mechanism. **What is the injection area mapping scheme for SuneKOS Cell 15?** The scheme uses 3 areas per side, 2.5ml per area, totalling 7.5ml per leg. Area A (trochanteric area) must always be injected combined with 2 other areas selected from Areas 1-5 based on the patient's presentation — covering thigh front, inner thigh, gluteus, and posterior thigh zones. **What does one pack of SuneKOS Cell 15 contain?** One pack of SuneKOS Cell 15 contains 1 treatment (15ml when reconstituted): 1x vial of Carbonate/Bicarbonate alkaline salts and 1x bottle of low molecular weight (200 KD) Sodium Hyaluronate/Amino Acids (HA/AA). **Is there a companion product recommended alongside SuneKOS Cell 15?** Yes. NUTRAKOS pH7 drinkable oral supplement is recommended as a daily companion throughout the entire SuneKOS Cell 15 treatment cycle. It provides the same HY6AA Amino Acid formula in oral form to systemically support the tissue environment and complement the injectable treatment from within. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### SuneKOS Cell 15 **Brand:** SuneKOS **Product type:** soft_product **Technical overview:** ## What is SuneKOS Cell 15? SuneKOS Cell 15 is an injectable CE Medical Device Class III for the treatment of **cellulite (Edematous Fibrosclerotic Panniculopathy — EFP)** in all four clinical stages. It is the only formula combining low molecular weight Hyaluronic Acid (HA), Amino Acids (AA), and **Carbonate/Bicarbonate alkaline salts** — uniquely addressing all three pathophysiological roots of cellulite simultaneously. Philosophy: **REBUILDING rather than DESTROYING** — promotes neo-collagenesis (not collagenase), microcirculation improvement, and pH re-equilibration of the tissue. --- ## Composition (Reconstituted as 15ml) - **1x vial:** Carbonate/Bicarbonate alkaline salts - **1x bottle:** Low molecular weight (200 KD) Sodium Hyaluronate / Amino Acids (HA/AA) - **One pack contains:** 1 treatment of 15ml --- ## Why Alkaline Salts? — The Acidosis Connection Cellulite involves tissue acidosis (reduced pH in subcutaneous layers) that drives chronic inflammation and progressive fibrosis. The Carbonate/Bicarbonate salts: - Rebalance the typical acidosis in latent inflammation characterising both early and late cellulite stages - Reduce fibrosis by re-equilibrating ECM inflammation - Complement the HA + AA action in promoting protein turnover optimisation No other cellulite injectable currently addresses this mechanism. --- ## Cellulite Stages & Treatment Techniques | Stage | Pathology | Technique | |---|---|---| | I & II | Edemato-inflammatory, hypo-oxygenation, acidosis | ATL-n (Needle) | | III & IV | Fibrosis, sclerosis, inflamm-aging | ATL-c (Cannula) | ### Stages I & II — ATL-n (Across Tension Lines — Needle) - Needle: 30G, 12mm | Inclination: 30° | Medium-Deep Dermis - 0.15ml per point | Perpendicularly to folding lines - Injection scheme: 3 areas per side, 2.5ml per area → **7.5ml per leg** ### Stages III & IV — ATL-c (Across Tension Lines — Cannula) - Cannula: 27G (40-50mm) or 22G (50-70mm) - Deep Dermis / Upper Hypodermis | Fan Technique | 0.8ml per injection - Injection scheme: 3 areas per side, 2.5ml per area → **7.5ml per leg** ### Injection Area Mapping Always inject **Area A** (trochanteric area) combined with 2 other areas selected from Areas 1-5 based on patient needs — covering thigh front, inner thigh, gluteus, and posterior thigh zones. 2.5ml per area. --- ## Treatment Protocols **Stages I & II:** - 3 sessions × 2-3 weeks apart (optional 4th session) - Maintenance: 1-2 sessions after 4-6 months - Repeat full cycle every 12 months **Stages III & IV:** - 4 sessions × 2-3 weeks apart (optional 5th session) - Maintenance: 1-2 sessions after 4-6 months - Repeat full cycle every 12 months **Complementary:** NUTRAKOS pH7 daily oral support throughout the entire treatment cycle. --- ## Clinical Study Results Preliminary study, 25 patients: Group A (11 patients, stages I-II) and Group B (14 patients, stages III-IV). Evaluation at baseline (T0), 1 month (T1), and 4 months (T4): | Measure | Group A | Group B | |---|---|---| | Visual Aspect Grade reduction (T1) | -47.5% | -27.0% | | Visual Aspect Grade reduction (T4) | -38.5% | -29.5% | | Thigh circumference reduction (T4) | -2.6% | -3.2% | | Ultrasound tissue depth (T1) | -4.0% | -13.5% | | Ultrasound tissue depth (T4) | -8.6% | -11.6% | Results maintained after 4 months in both groups. **Unique features:** Only cellulite injectable with triple-action formula: HA + AA + Carbonate/Bicarbonate alkaline salts. Simultaneously addresses ECM disruption, microcirculation AND tissue acidosis. Covers all 4 EFP stages with stage-specific techniques (ATL-n / ATL-c). REBUILDING not destroying. 15ml per treatment. CE Class III. **Clinical indications:** - cellulite - EFP - edematous fibrosclerotic panniculopathy - orange peel skin - skin dimpling - thigh cellulite - gluteal cellulite - body contouring - tissue acidosis - skin fibrosis - microcirculation - body laxity **Positioning:** Also known as: SuneKOS Cell 15, SK Cell 15, sunekos cell, cellulite injectable sunekos, sunekos cell dubai. Compared against: Alidya, Toskani Cellulite, PPC injections, phosphatidylcholine, carboxytherapy cellulite, mesotherapy cellulite. **Clinician FAQs:** **What is SuneKOS Cell 15 and what makes it different from other cellulite treatments?** SuneKOS Cell 15 is an injectable CE Medical Device Class III for all 4 stages of cellulite (EFP). It is the only formula combining HA, Amino Acids, AND Carbonate/Bicarbonate alkaline salts — addressing three root causes simultaneously: ECM disruption (HA + AA rebuild collagen and elastin), poor microcirculation, and tissue acidosis (alkaline salts rebalance pH). Its philosophy is REBUILDING rather than DESTROYING — promoting neo-collagenesis, not collagenase breakdown. **How many treatment sessions are needed and what is the maintenance protocol?** For Stages I & II: 3 sessions spaced 2-3 weeks apart (optional 4th). For Stages III & IV: 4 sessions spaced 2-3 weeks apart (optional 5th). Maintenance for both groups: 1-2 sessions after 4-6 months. The full treatment cycle should be repeated every 12 months. Daily support with NUTRAKOS pH7 is recommended throughout the programme. **What clinical results has SuneKOS Cell 15 demonstrated?** In a preliminary study of 25 patients: Group A (stages I-II, 11 patients) showed -47.5% reduction in visual aspect grade at 1 month and -38.5% at 4 months. Group B (stages III-IV, 14 patients) showed -27% at 1 month and -29.5% at 4 months. Thigh circumference reduced by up to -3.2% and ultrasound-measured tissue depth by up to -13.5%. Results were maintained after 4 months in both groups. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### SuneKOS Cell 15 **Brand:** SuneKOS **Type:** soft_product **Portfolio status:** direct portfolio ## What is SuneKOS Cell 15? **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. _Note: listed in the internal KB only — no public product page._ ## Product: NutraKOS Drinkable **Brand:** SuneKOS ### For patients ### NutraKOS Drinkable ## What is NutraKOS Drinkable? **What it treats:** skin aging, skin hydration, collagen support, elastin support, hair nails, oral beauty supplement, photoaging, skin elasticity, skin firmness, skin smoothness, anti-aging oral. **Questions patients commonly ask:** **What is NutraKOS Drinkable and how does it relate to the SuneKOS injectables?** NutraKOS Drinkable is a patented oral food supplement by Professional Dietetics SpA — the same manufacturer as SuneKOS. It contains the same HY6AA PLAAT FORM amino acid formula as the SuneKOS injectables (Glycine, L-Proline, L-Lysine, L-Alanine, L-Valine, L-Leucine), delivering the same collagen and elastin-stimulating building blocks systemically through daily oral intake. It is the ideal nutritional companion to the injectable treatments. **What are the benefits of NutraKOS Drinkable?** NutraKOS Drinkable improves skin elasticity and hydration, maintains and protects overall skin wellbeing, and preserves healthy hair and nails. It provides systemic amino acid support for the Extra Cellular Matrix (ECM) and complements and extends the results of SuneKOS injectable treatments. **How is NutraKOS Drinkable taken?** Dissolve 1 stickpack in a glass of water or cold beverage, or take directly without dilution. During Weeks 1-2: take 2 stickpacks per day (one at lunch and one at dinner). From Week 3 through Week 13: take 1 stickpack per day. Repeat every season. **What does one box of NutraKOS Drinkable contain?** One box of NutraKOS Drinkable contains 30 stickpacks. The formula is sugar free and uses the patented HY6AA amino acid combination. Manufactured by Professional Dietetics SpA in Milan, Italy. **What clinical results has NutraKOS Drinkable demonstrated?** A pilot study on 12 female volunteers (age 39-62) showed statistically significant skin hydration improvements at 2 weeks: +8.5% at 0.5mm depth and +4.4% at 1.5mm depth on the volar surface, maintained at 1 month. Plastoelasticity (skin firmness/elasticity) improved significantly: -26.8% Uv at 2 weeks and -24.2% at 1 month. Volunteer self-assessment at 1 month: 92% reported improved smoothness, 83% improved firmness, 83% improved hydration. Tolerance was 100% good or excellent with no adverse events. **Is NutraKOS Drinkable recommended alongside SuneKOS Cell 15?** Yes. NutraKOS is specifically recommended as NUTRAKOS pH7 daily oral support throughout the entire SuneKOS Cell 15 cellulite treatment cycle. It provides systemic nutritional and pH support to complement the injectable action from within, reinforcing the tissue environment being treated by Cell 15. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### NutraKOS Drinkable **Brand:** SuneKOS **Product type:** soft_product **Technical overview:** ## What is NutraKOS Drinkable? NutraKOS Drinkable is a patented oral food supplement developed by Professional Dietetics SpA (Milan, Italy) — the same manufacturer behind the SuneKOS injectable line. It delivers the same HY6AA PLAAT FORM amino acid formula in oral form, providing systemic nutritional support for skin, hair, and nails from within. NutraKOS is the ideal companion product to the SuneKOS injectable range, supporting and extending the biological effects of the injectable treatments between and during sessions. --- ## Composition & Format - **Format:** Stickpacks (powder sachets dissolved in water or cold beverage) - **Pack size:** 30 stickpacks per box - **Sugar free** - **Patented formula** (same HY6AA PLAAT FORM amino acid cluster as SuneKOS injectables) - **Manufacturer:** Professional Dietetics SpA, Milan, Italy ### The 6 Amino Acids (HY6AA): - **Glycine, L-Proline, L-Lysine** — Collagen Amino Acids - **L-Alanine, L-Valine** — Elastin Amino Acids - **L-Leucine** — Prosynthetic Amino Acid --- ## Directions for Use - Dissolve 1 stickpack in a glass of water or cold beverage - Can also be taken directly without dilution - **Weeks 1-2:** 2 stickpacks per day (lunch + dinner) - **Weeks 3-13:** 1 stickpack per day - Repeat every season --- ## Benefits - Improves skin elasticity and hydration - Maintains and protects overall skin wellbeing - Preserves healthy hair and nails - Systemic amino acid support for the ECM - Complements and extends SuneKOS injectable results --- ## Companion Use with SuneKOS Cell 15 NutraKOS is specifically recommended as **NUTRAKOS pH7** daily oral support throughout the entire SuneKOS Cell 15 cellulite treatment cycle, providing systemic pH and nutritional support to complement the injectable action. --- ## Clinical Study Results Pilot study — 12 female volunteers, age 39-62, Fitzpatrick II-III, 1 month duration. Evaluations at baseline (T0), 2 weeks (T2W), and 1 month (T1M): ### Skin Hydration — Volar Surface | Depth | T2W | T1M | |---|---|---| | 0.5mm | +8.5% | +8.0% | | 1.5mm | +4.4% | +6.5% | Both results statistically significant. ### Skin Hydration — Dorsal Surface (trend) | Depth | T2W | T1M | |---|---|---| | 0.5mm | +7.6% | — | | 1.5mm | — | +5.9% | ### Plastoelasticity (Uv — superficial & deep) - Superficial plastoelasticity dorsal (Uv): **-26.8% at T2W**, **-25.1% at T1M** — statistically significant - Deep plastoelasticity volar (Uv): **-24.2% at T1M** — statistically significant *(Lower Uv = improved elasticity)* ### Volunteer Self-Assessment at T1M | Parameter | % Reporting Improvement | |---|---| | Smoothness | 92% | | Firmness | 83% | | Hydration | 83% | | Suppleness | 67% | | Microrelief | 67% | ### Tolerance - 100% good or excellent tolerance - No adverse events recorded ### Superiority vs Hydrolysed Collagen NutraKOS demonstrated statistically significant results at **2 weeks** — versus hydrolysed collagen products which typically require 4 weeks or more to show measurable effects. **Unique features:** Oral companion to the full SuneKOS injectable range. Same patented HY6AA PLAAT FORM formula in drinkable form. Statistically significant skin hydration results at 2 weeks — faster than hydrolysed collagen. 30 stickpacks per box. Sugar free. Recommended daily alongside SuneKOS Cell 15. **Clinical indications:** - skin aging - skin hydration - collagen support - elastin support - hair nails - oral beauty supplement - photoaging - skin elasticity - skin firmness - skin smoothness - anti-aging oral **Positioning:** Also known as: NutraKOS, Nutrakos pH7, nutrakos drinkable, nutrakos sunekos, HY6AA oral, sunekos oral supplement. Compared against: Skinade, Imedeen, Perfectil, Viviscal, hydrolysed collagen supplements, Dose & Co collagen, The Beauty Chef. **Clinician FAQs:** **What clinical results has NutraKOS Drinkable demonstrated?** A pilot study on 12 female volunteers (age 39-62) showed statistically significant skin hydration improvements at 2 weeks: +8.5% at 0.5mm depth and +4.4% at 1.5mm depth on the volar surface, maintained at 1 month. Plastoelasticity (skin firmness/elasticity) improved significantly: -26.8% Uv at 2 weeks and -24.2% at 1 month. Volunteer self-assessment at 1 month: 92% reported improved smoothness, 83% improved firmness, 83% improved hydration. Tolerance was 100% good or excellent with no adverse events. **How does NutraKOS compare to hydrolysed collagen supplements?** NutraKOS demonstrated statistically significant improvements in skin hydration and elasticity at 2 weeks. Hydrolysed collagen products typically require 4 weeks or more to show measurable effects. This faster onset is attributed to the precise HY6AA PLAAT FORM amino acid ratio, which is specifically formulated to directly stimulate fibroblast activity rather than relying on general collagen peptide supplementation. **Can NutraKOS Drinkable be used on its own without any SuneKOS injectable?** Yes. NutraKOS Drinkable can be used as a standalone daily supplement for skin, hair, and nail health. It is suitable as a preventative and maintenance supplement for patients who wish to support their skin from within without injectable treatment, or as a seasonal maintenance supplement between injectable treatment cycles. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### NutraKOS Drinkable **Brand:** SuneKOS **Type:** soft_product **Portfolio status:** direct portfolio ## What is NutraKOS Drinkable? **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. _Note: listed in the internal KB only — no public product page._ ## Product: AnteAGE **Brand:** AnteAGE ### For patients ### AnteAGE AnteAGE is the world's most advanced regenerative skincare brand, built on 11+ years of Bone Marrow Stem Cell research. Developed by Cellese Biological Lab in the USA and distributed exclusively in the Middle East by DUBIMED, AnteAGE offers professional lines that harness the biological intelligence of stem cell-derived signals to restore the skin's and scalp's youthful healing capacity. **What it treats:** anti-aging, skin rejuvenation, collagen rebuilding, skin tightening, hair loss treatment, skin brightening, hyperpigmentation, fine lines and wrinkles, acne scars, skin texture, pore reduction, post-treatment healing, wound healing acceleration, skin vitality. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### AnteAGE **Brand:** AnteAGE **Product type:** brand **Technical overview:** AnteAGE is the world's most advanced regenerative skincare brand, built on 11+ years of Bone Marrow Stem Cell research. Developed by Cellese Biological Lab in the USA and distributed exclusively in the Middle East by DUBIMED, AnteAGE offers professional lines that harness the biological intelligence of stem cell-derived signals to restore the skin's and scalp's youthful healing capacity. The science behind AnteAGE is rooted in the understanding that as we age, growth factor and cytokine levels decline — stripping skin of its ability to self-repair. AnteAGE restores these signals at the cellular level, reversing the aging phenotype without synthetic chemicals or harsh ingredients. AnteAGE offers four professional product families available through DUBIMED: 1. ANTEAGE MDX BIOSOME™ — Biomimetic Exosomes (synthetic, non-human-derived, room-temperature stable). Available in Skin, Brightening, and Hair formulations. FDA MoCRA registered. Contains 25 Billion Biosomes per treatment. 2. ANTEAGE MDX EXOSOME™ — Real Bone Marrow Stem Cell Exosomes. 5 Billion real exosomes per treatment. The only exosome in the world sourced exclusively from Bone Marrow Stem Cells. 300% more potent than standard growth factor solutions. Refrigerated 2°C–8°C. 3. ANTEAGE MD™ — Professional in-clinic microneedling solutions. Skin, Brightening, and Hair clinical treatment systems. For use with dermal needling, RF needling, and energy-based treatments. 4. ANTEAGE MD HOME CARE™ — Daily maintenance system for home use. Serum, Accelerator, Brightener, Hair SCS, and Hair Polybotanical. Extends and maintains in-clinic treatment results. All AnteAGE products are manufactured in an ISO 7 Class Clean Room Facility, GMP Certified, and backed by academic partnerships with UC Irvine Stem Cell Research Center, City of Hope, NIH, Cleveland Clinic, and Dallas Plastic Surgery Institute. **Unique features:** 1. TWO DISTINCT EXOSOME TECHNOLOGIES IN ONE BRAND: AnteAGE is the only brand in the world offering both real Bone Marrow Stem Cell Exosomes (MDX Exosome) and engineered Biomimetic Exosomes (MDX Biosome) — giving clinicians the choice between the most advanced naturally-derived exosome and the most advanced synthetic exosome, both from the same trusted source. 2. 11+ YEARS OF BONE MARROW STEM CELL RESEARCH: Cellese has been culturing Bone Marrow Stem Cells for over 11 years — longer than any other exosome company in aesthetics. This gives unmatched expertise in growth factor ratios and cytokine profiles. 3. ISO 7 CLASS CLEAN ROOM + GMP CERTIFIED MANUFACTURING: All products manufactured in an ISO 7 Class Clean Room — the same standard used for pharmaceutical manufacturing. GMP Certified, California State Seal registered. 4. COMPLETE ECOSYSTEM: IN-CLINIC + HOME CARE: The only regenerative brand offering a complete clinical-to-home continuum: professional in-clinic solutions (MDX Biosome, MDX Exosome, MD Clinical) + home maintenance (MD Home Care). 5. ACADEMIC & MEDICAL INSTITUTIONAL BACKING: Academic: UC Irvine Stem Cell Research Center | City of Hope | NIH National Institutes on Aging. Medical: Cleveland Clinic | Center for Dermatology and Laser Surgery | Dallas Plastic Surgery Institute | Richard L. Zeef M.D. | Vancouver Laser & Skin Care Centre. **Clinical indications:** - anti-aging - skin rejuvenation - collagen rebuilding - skin tightening - hair loss treatment - skin brightening - hyperpigmentation - fine lines and wrinkles - acne scars - skin texture - pore reduction - post-treatment healing - wound healing acceleration - skin vitality **Positioning:** Also known as: AnteAGE, Ante AGE, Anti Age, AnteAGE MDX, AnteAGE MD, AnteAGE Middle East, Anteage ME, أنتي إيج, أنتي آج, AnteAGE Biosome, AnteAGE Exosome, AnteAGE Cellese. Compared against: PRP, PRF, Rejuran, Juvelook, Polynucleotides, PDRN, Benev, RejuvaMD, ProCell, Skinceuticals, SkinBetter, Dermapen MG7, growth factor serum. **Clinician FAQs:** **What is AnteAGE and what products does it offer?** AnteAGE is an American regenerative skincare brand developed by Cellese Biological Lab, built on over 11 years of Bone Marrow Stem Cell research. It is distributed in the Middle East exclusively by DUBIMED. Four professional product families: 1. AnteAGE MDX Biosome — Biomimetic synthetic exosomes. 25 Billion Biosomes per treatment. Skin, Brightening, and Hair formulations. Room temperature stable. FDA MoCRA registered. 2. AnteAGE MDX Exosome — Real Bone Marrow Stem Cell exosomes. 5 Billion real exosomes. Refrigerated. 300% more potent than standard GF solutions. 3. AnteAGE MD — Professional in-clinic microneedling solutions for Skin, Brightening, and Hair. 4. AnteAGE MD Home Care — Daily home maintenance: Serum, Accelerator, Brightener, Hair SCS, Hair Polybotanical. All products: Made in USA | ISO 7 Clean Room | GMP Certified. **What is the difference between AnteAGE MDX Biosome and AnteAGE MDX Exosome?** AnteAGE MDX Biosome (Biomimetic/Synthetic): - Engineered lipid nanoparticles (100nm) loaded with recombinant human proteins — not derived from human cells - 25 Billion Biosomes per treatment (5x more particles than Exosome) - Room temperature stable — no cold chain required - FDA MoCRA #53-603116-583651 registered - Dual source: Bone Marrow + Umbilical Cord signals - ~500% more biological signal concentration than GF alone - Three specialized formulations: Skin, Brightening, Hair AnteAGE MDX Exosome (Real/Natural): - Real Bone Marrow Stem Cell-derived exosomes — the only such product in the world - 5 Billion real exosomes per treatment | 6,000 unique growth factors per vial - 300% more potent than standard GF solution - Refrigerated 2°C–8°C | Zero allergens - Verified at 100nm by independent QNANO particle analysis Both achieve equivalent biological activity in vitro. Choose Biosome for stability, logistics ease, and higher particle count. Choose Exosome for maximum biological complexity and 6,000 natural growth factors. **Where are AnteAGE products made and what certifications do they hold?** All AnteAGE products are Made in USA by Cellese Biological Lab, manufactured in an ISO 7 Class Clean Room Facility — the same standard used in pharmaceutical manufacturing. Certifications: - GMP Certified | California State Seal | EUIPO registered trademark - FDA MoCRA #53-603116-583651 (Biosome — registered July 2024) - NAMSA OECD 471 Cell Safe Testing (Biosome) - Independent particle verification QNANO, Irvine USA (Exosome — confirmed 100nm real exosomes) Academic affiliations: UC Irvine Stem Cell Research Center | City of Hope | NIH (National Institutes on Aging) Medical affiliations: Cleveland Clinic | Center for Dermatology and Laser Surgery | Dallas Plastic Surgery Institute | Richard L. Zeef M.D. | Vancouver Laser & Skin Care Centre **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### AnteAGE **Brand:** AnteAGE **Type:** brand **Portfolio status:** direct portfolio AnteAGE is the world's most advanced regenerative skincare brand, built on 11+ years of Bone Marrow Stem Cell research. Developed by Cellese Biological Lab in the USA and distributed exclusively in the Middle East by DUBIMED, AnteAGE offers professional lines that harness the biological intelligence of stem cell-derived signals to restore the skin's and scalp's youthful healing capacity. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. **Strategic FAQs:** **What is AnteAGE and what products does it offer?** AnteAGE is an American regenerative skincare brand developed by Cellese Biological Lab, built on over 11 years of Bone Marrow Stem Cell research. It is distributed in the Middle East exclusively by DUBIMED. Four professional product families: 1. AnteAGE MDX Biosome — Biomimetic synthetic exosomes. 25 Billion Biosomes per treatment. Skin, Brightening, and Hair formulations. Room temperature stable. FDA MoCRA registered. 2. AnteAGE MDX Exosome — Real Bone Marrow Stem Cell exosomes. 5 Billion real exosomes. Refrigerated. 300% more potent than standard GF solutions. 3. AnteAGE MD — Professional in-clinic microneedling solutions for Skin, Brightening, and Hair. 4. AnteAGE MD Home Care — Daily home maintenance: Serum, Accelerator, Brightener, Hair SCS, Hair Polybotanical. All products: Made in USA | ISO 7 Clean Room | GMP Certified. _Note: listed in the internal KB only — no public product page._ ## Product: dermamelan **Brand:** MESOESTETIC ### For patients ### dermamelan dermamelan is mesoestetic's most advanced professional depigmentation treatment, specifically designed for the most severe and recurrent cases of melasma and stubborn hyperpigmentation. It operates on the same proven dual-phase methodology as cosmelan but with a significantly more intensive formulation and higher concentration of active depigmenting agents. Phase 1 is an in-clinic professional mask (dermamelan 1) with elevated concentrations of azelaic acid, kojic acid, phytic acid, retinol, and ascorbic acid combined with arbutin for maximum tyrosinase inhibition. Phase 2 comprises an extended homecare protocol (dermamelan 2 treatment cream) used over 6-12 months to maintain results and prevent melanin rebound. dermamelan acts on all stages of the melanogenesis process — it regulates melanocyte activation, inhibits tyrosinase enzymatic activity, blocks melanin transfer to keratinocytes, and promotes controlled desquamation of pigmented cells. The treatment is clinically validated for severe melasma (including hormonal and mixed types), chronic post-inflammatory hyperpigmentation, and refractory cases that have not responded to other treatments. It is suitable for all Fitzpatrick skin types (I-VI) with particular strength in treating darker skin phototypes. Results are visible within 2-3 weeks with progressive improvement over the full protocol duration. **What it treats:** melasma, pigmentation, discoloration, severe melasma, recurrent melasma, hormonal melasma, post-inflammatory hyperpigmentation, refractory pigmentation, dark spots, chloasma. **Questions patients commonly ask:** **What results can patients with severe melasma expect from dermamelan and how does it differ from cosmelan?** dermamelan is mesoestetic's most intensive depigmentation protocol, specifically engineered for severe, recurrent, and treatment-resistant melasma. Patients can expect up to 99% reduction in pigmentation intensity, with visible improvement starting from week 2–3. Compared to cosmelan, dermamelan contains higher concentrations of active depigmenting agents and includes a more rigorous home-care maintenance phase to prevent rebound hyperpigmentation. The treatment is safe for all skin phototypes when administered by trained professionals, though patients should expect moderate peeling and redness during the first 5–7 days. Long-term results are maintained through the continuous home protocol and strict sun protection. **What is dermamelan?** Dermamelan is a depigmentation method from mesoestetic built on more than 30 years of research and clinical experience and designed to target visible pigmentation and its underlying causes. **How is dermamelan positioned on the DUBIMED page?** The page presents dermamelan as an advanced depigmentation solution developed from long-term research and clinical expertise. **Where to get this treatment in the UAE / GCC:** speak to a DUBIMED-partnered clinic. Contact details on the DUBIMED site. ### For clinicians ### dermamelan **Brand:** MESOESTETIC **Product type:** soft_product **Technical overview:** dermamelan is mesoestetic's most advanced professional depigmentation treatment, specifically designed for the most severe and recurrent cases of melasma and stubborn hyperpigmentation. It operates on the same proven dual-phase methodology as cosmelan but with a significantly more intensive formulation and higher concentration of active depigmenting agents. Phase 1 is an in-clinic professional mask (dermamelan 1) with elevated concentrations of azelaic acid, kojic acid, phytic acid, retinol, and ascorbic acid combined with arbutin for maximum tyrosinase inhibition. Phase 2 comprises an extended homecare protocol (dermamelan 2 treatment cream) used over 6-12 months to maintain results and prevent melanin rebound. dermamelan acts on all stages of the melanogenesis process — it regulates melanocyte activation, inhibits tyrosinase enzymatic activity, blocks melanin transfer to keratinocytes, and promotes controlled desquamation of pigmented cells. The treatment is clinically validated for severe melasma (including hormonal and mixed types), chronic post-inflammatory hyperpigmentation, and refractory cases that have not responded to other treatments. It is suitable for all Fitzpatrick skin types (I-VI) with particular strength in treating darker skin phototypes. Results are visible within 2-3 weeks with progressive improvement over the full protocol duration. **Unique features:** mesoestetic's most potent depigmentation protocol designed for severe and recurrent melasma cases. Higher concentration of active depigmenting agents compared to cosmelan, including added arbutin for enhanced tyrosinase inhibition. Acts on all four stages of melanogenesis: melanocyte activation, tyrosinase activity, melanin transfer, and pigmented cell desquamation. Extended 6-12 month homecare protocol for sustained results and rebound prevention. Clinically validated for treatment-resistant hyperpigmentation cases. Particularly effective on Fitzpatrick IV-VI skin types where other depigmentation methods carry higher risk. Visible results within 2-3 weeks with progressive improvement throughout the protocol. **Clinical indications:** - melasma - pigmentation - discoloration - severe melasma - recurrent melasma - hormonal melasma - post-inflammatory hyperpigmentation - refractory pigmentation - dark spots - chloasma **Positioning:** Also known as: cosmelan. Compared against: depigmenting treatment. **Clinician FAQs:** **What results can patients with severe melasma expect from dermamelan and how does it differ from cosmelan?** dermamelan is mesoestetic's most intensive depigmentation protocol, specifically engineered for severe, recurrent, and treatment-resistant melasma. Patients can expect up to 99% reduction in pigmentation intensity, with visible improvement starting from week 2–3. Compared to cosmelan, dermamelan contains higher concentrations of active depigmenting agents and includes a more rigorous home-care maintenance phase to prevent rebound hyperpigmentation. The treatment is safe for all skin phototypes when administered by trained professionals, though patients should expect moderate peeling and redness during the first 5–7 days. Long-term results are maintained through the continuous home protocol and strict sun protection. **DUBIMED support:** training (foundation + advanced + on-site), biomedical service, parts & consumables, clinical protocol support. GCC territory (UAE, Qatar, Oman, Saudi Arabia). ### For strategic buyers ### dermamelan **Brand:** MESOESTETIC **Type:** soft_product **Portfolio status:** direct portfolio dermamelan is mesoestetic's most advanced professional depigmentation treatment, specifically designed for the most severe and recurrent cases of melasma and stubborn hyperpigmentation. It operates on the same proven dual-phase methodology as cosmelan but with a significantly more intensive formulation and higher concentration of active depigmenting agents. Phase 1 is an in-clinic professional mask (dermamelan 1) with elevated concentrations of azelaic acid, kojic acid, phytic acid, retinol, and ascorbic acid combined with arbutin for maximum tyrosinase inhibition. Phase 2 comprises an extended homecare protocol (dermamelan 2 treatment cream) used over 6-12 months to maintain results and prevent melanin rebound. dermamelan acts on all stages of the melanogenesis process — it regulates melanocyte activation, inhibits tyrosinase enzymatic activity, blocks melanin transfer to keratinocytes, and promotes controlled desquamation of pigmented cells. The treatment is clinically validated for severe melasma (including hormonal and mixed types), chronic post-inflammatory hyperpigmentation, and refractory cases that have not responded to other treatments. It is suitable for all Fitzpatrick skin types (I-VI) with particular strength in treating darker skin phototypes. Results are visible within 2-3 weeks with progressive improvement over the full protocol duration. **Distribution:** available through DUBIMED across UAE, Qatar, Oman, and Saudi Arabia. _Note: listed in the internal KB only — no public product page._ --- ## Services ### Clinical Training **URL:** https://dubaimed.com/clinical-training Hands-on clinical training, workshops, and onboarding for aesthetic and dermatology practices across the UAE, Qatar, Oman, and Saudi Arabia. Formats: foundation training (1-2 days), advanced certification (3-5 days), half-day workshops, on-site at clinic, and at DUBIMED facilities. Deliverables: certificate of completion, lifetime access to the online training platform, post-training protocol support. ### Biomedical Service **URL:** https://dubaimed.com/biomedical-service Device maintenance, calibration, and technical support for every medical and aesthetic device distributed by DUBIMED. Covers preventive maintenance, performance verification, on-site and in-workshop repair, parts sourcing, warranty management, and uptime SLAs. Engineers are factory-trained by the brands DUBIMED represents. ### Logistics & Distribution **URL:** https://dubaimed.com/logistics-distribution End-to-end distribution of medical and aesthetic products across the UAE, Qatar, Oman, and Saudi Arabia. Includes customs clearance and regulatory filing, cold-chain handling for temperature-sensitive biologics, clinic-ready delivery coordinated with training days, and stock management for consumables. ### Marketing Support **URL:** https://dubaimed.com/marketing-support Co-marketing, event support, and clinic-facing campaign assets for brands DUBIMED represents. Includes joint marketing campaigns, patient-facing collateral in English and Arabic, events and masterclasses, digital support (social, paid-ad creative, landing pages), and the DUBIMED Stars loyalty program. --- ## Patient landing pages — English ### AnteAGE Biosome **URL:** https://dubaimed.com/patient/anteage-biosome - **Language:** English Biosome activates your skin and hair cells from within, helping them repair, renew, and function at their best. It supports stronger hair, healthier skin, and visible improvement over time by boosting the body’s natural regeneration process. ### Sofwave **URL:** https://dubaimed.com/patient/sofwave - **Language:** English Discover Sofwave, a non-invasive ultrasound treatment that lifts eyebrows, tightens the jawline and neck, and reduces wrinkles. Book your consultation at trusted clinics in the UAE. --- ## Patient landing pages — Arabic ### سوفويف (Arabic) **URL:** https://dubaimed.com/ar/patient/sofwave - **Language:** Arabic تعرف على علاج سوفويف لشد البشرة بدون جراحة باستخدام تقنية الموجات فوق الصوتية. يساعد على رفع الحاجبين وشد الرقبة وتقليل التجاعيد. احجز استشارتك الآن. ### آنتي آج بايوزوم (Arabic) **URL:** https://dubaimed.com/ar/patient/anteage-biosome - **Language:** Arabic اكتشف علاج بايوزوم من دوبيميد لدعم تجدد خلايا البشرة وتحسين جودة الجلد وتقوية نمو الشعر. علاج متوفر في عيادات متخصصة في الإمارات وقطر وعُمان. --- ## Media center articles ### Aesthetic Medical Supplies Dubai UAE **URL:** https://dubaimed.com/media-center/aesthetic-medical-supplies-dubai-uae - **Category:** blog - **Published:** 2026-02-05 - **Tags:** Aesthetic Medical Supplies, Medical Equipment Dubai, Healthcare Distribution UAE, Aesthetic Devices, Medical Products GCC DUBIMED is the leading supplier of aesthetic medical equipment and supplies in Dubai, UAE, and the GCC region. With over 40 years of experience, ISO 9001:2015 certification, and authorized distributor status for 15+ premium brands including Sofwave, Galderma, and Ultraformer, DUBIMED provides comprehensive solutions including devices, injectables, clinical training, biomedical support, and same-day delivery across the UAE. ### Marketing Support for Aesthetic Clinics Dubai UAE **URL:** https://dubaimed.com/media-center/marketing-support-for-aesthetic-clinics-dubai-uae - **Category:** blog - **Published:** 2026-02-04 - **Tags:** marketing support Dubai, aesthetic clinic marketing UAE, medical practice marketing Dubai, clinic branding Dubai, patient acquisition strategies UAE DUBIMED provides comprehensive marketing support services for aesthetic medical clinics across Dubai, UAE, and the GCC. Through tailored marketing strategies combining physical and digital channels, DUBIMED empowers practices to enhance brand visibility, attract new patients, and strengthen competitive positioning. Services include patient education materials, digital marketing, social media management, branding, referral programs, and marketing training. Proprietary B2C2B hybrid strategy drives both consumer demand and professional referrals for sustainable growth. ### Logistics & Distribution Dubai UAE **URL:** https://dubaimed.com/media-center/logistics-and-distribution-dubai-uae - **Category:** blog - **Published:** 2026-02-02 - **Tags:** Logistics and distribution Dubai, Equipment distribution, Healthcare logistics DUBIMED operates comprehensive logistics and distribution for aesthetic medical equipment across Dubai, UAE, and the GCC. With 10,000+ annual deliveries and 99% on-time rate, DUBIMED ensures seamless operations and timely deliveries. GDP certified for pharmaceutical-grade handling. Services include same-day Dubai delivery, temperature-controlled transport, secure warehousing, inventory management, and emergency delivery. Coverage throughout UAE, Qatar, Oman, and Saudi Arabia with specialized handling for devices, injectables, and consumables. ### Clinical Training Dubai UAE **URL:** https://dubaimed.com/media-center/clinical-training-dubai-uae - **Category:** blog - **Published:** 2026-02-01 - **Tags:** Clinical Training, Aesthetic Device Training, Healthcare Education UAE, Professional Development, Device Certification DUBIMED provides comprehensive clinical training for aesthetic medical devices across Dubai, UAE, and the GCC. With 8+ years of training operations and 3,000+ sessions delivered, DUBIMED's certified specialists—each with 10+ years of experience—empower practitioners with advanced techniques, hands-on training, and ongoing support for devices including Sofwave, Ultraformer, lasers, RF systems, and injectables. ### DUBIMED Kids Academy Season 3 **URL:** https://dubaimed.com/media-center/dubimed-kids-academy-season-3 - **Category:** events - **Published:** 2025-12-16 - **Tags:** Kids Academy, Kids Academy Season 3, DUBIMED CSR DUBIMED Kids Academy Season 3 brought children into real-world science through hands-on experiments, clinic visits, and immersive medical learning. ### DUBIMED x CLASSYS Present VOLFOMER **URL:** https://dubaimed.com/media-center/dubimed-x-classys-present-volfomer - **Category:** events - **Published:** 2025-11-06 - **Tags:** VOLFORMER, Ultraformer MPT, Volnewmer, Classys DUBIMED and CLASSYS hosted the VOLFOMER scientific launch at Bulgari Resort Dubai, featuring Dr. Boncheol Leo Goo and leading dermatologists sharing clinical experience with Ultraformer MPT and Volnewmer combination therapy. ### DUBIMED x MEIDAM 2025 **URL:** https://dubaimed.com/media-center/dubimed-x-meidam-2025 - **Category:** events - **Published:** 2025-10-31 - **Tags:** mediam, ge healthcare DUBIMED proudly participated as Pearl Sponsor at the MEIDAM Congress 2025, the leading regional meeting in dermatology and aesthetic medicine. This year marked a historic milestone as DUBIMED officially became a GE Healthcare distributor, launching the revolutionary VScan™ and Venue Lines™ ultrasound solutions. ### VYDENCE – Try it once, Love it Forever! **URL:** https://dubaimed.com/media-center/vydence-try-it-once-love-it-forever - **Category:** news - **Published:** 2025-10-23 - **Tags:** vydence, medical device, etherea mx, zye For over 40 years, Vydence Medical has led the evolution of laser technology in aesthetic medicine. Driven by a commitment to efficacy, versatility, and profitability, we continue to set new benchmarks in innovation, clinical excellence, and business success. ### SuneKOS Global Summit 2025 **URL:** https://dubaimed.com/media-center/sunekos-global-summit-2025 - **Category:** events - **Published:** 2025-09-27 - **Tags:** sunekos global summit, sunekos event A Landmark Gathering in Regenerative and Aesthetic Medicine Dubai, UAE – September 27–28, 2025 – DUBIMED proudly hosted the SuneKOS Global Summit 2025, a two-day event that brought together more than 350 medical professionals, key opinion leaders, and distributors from around the world. ### DUBIMED x Beauty & Beyond Summit 2025 **URL:** https://dubaimed.com/media-center/dubimed-x-beauty-and-beyond-summit-2025 - **Category:** events - **Published:** 2025-09-05 - **Tags:** beauty & beyond DUBIMED proudly participated in the prestigious Beauty & Beyond Summit 2025, one of the region’s most anticipated gatherings for aesthetic medicine, skincare, and anti-aging solutions. The event brought together leading experts, physicians, and industry professionals to explore the latest breakthroughs in regenerative medicine, dermatology, and medical aesthetics. ### DUBIMED X Dubai Derma 2025 **URL:** https://dubaimed.com/media-center/dubimed-x-dubai-derma-2025 - **Category:** events - **Published:** 2025-04-16 - **Tags:** dubai derma, classys, ultraformer, ultraformer mpt DUBIMED made a powerful impact at Dubai Derma 2025 with the event’s largest pavilion, uniting all brands at Hall 8, booths 8D01 and 8D05. ### DUBIMED Exclusive Distributor Ultraformer **URL:** https://dubaimed.com/media-center/dubimed-exclusive-distributor-ultraformer - **Category:** news - **Published:** 2025-04-01 DUBIMED has proudly announced its appointment as the exclusive distributor for CLASSYS devices in the UAE, Qatar, and Oman. This partnership includes the renowned Ultraformer MPT and Ultraformer III systems. ### Biomedical Service Dubai UAE **URL:** https://dubaimed.com/media-center/biomedical-service-dubai-uae - **Category:** blog - **Published:** 2025-01-29 - **Tags:** Biomedical Service, Equipment Maintenance, Medical Equipment Service UAE, Healthcare Engineering, Preventative Maintenance DUBIMED provides comprehensive biomedical engineering services and medical equipment maintenance for aesthetic devices across Dubai, UAE, and the GCC. With highly skilled engineers and technicians, DUBIMED delivers fast, efficient service including installation, preventative maintenance, repairs, and 24/7 emergency support. Same-day service available in Dubai. Authorized service provider for Sofwave, Ultraformer, lasers, RF systems, and 15+ premium brands. Genuine parts, manufacturer standards, minimal downtime. ### Dubimed Kickoff Meeting: GIT’25 **URL:** https://dubaimed.com/media-center/dubimed-git25 - **Category:** events - **Published:** 2025-01-25 The kickoff meeting set the tone for the year ahead, aligning every department with a shared vision of transformation, excellence, and impact. ### DUBIMED at the Beauty and Beyond Conference 2024 **URL:** https://dubaimed.com/media-center/dubimed-beauty-and-beyond-conference-2024 - **Category:** events - **Published:** 2024-10-15 DUBIMED a leader in innovative medical and aesthetic solutions, recently participated in the prestigious Beauty and Beyond Summit held on 12-13 October 2024 at the Al Habtoor Palace in Dubai. ### DUBIMED × MEIDAM 2024 **URL:** https://dubaimed.com/media-center/dubimed-meidam-2024 - **Category:** events - **Published:** 2024-09-24 DUBIMED made a remarkable impact at MEIDAM 2024, the prestigious Middle East International Dermatology & Aesthetic Medicine Conference, held in Dubai from November 15 to 17, 2024. ### Ellacor Technology by DUBIMED| Reshaping the future **URL:** https://dubaimed.com/media-center/dubimed-distributor-for-ellacor - **Category:** events - **Published:** 2024-05-01 We are thrilled to announce that Dubimed is now the official distributor in the region for Ellacor, the revolutionary scarless skin removal and lifting technology invented by Harvard. ### DUBIMED Introduces SkinPen Precision by Crown Aesthetics **URL:** https://dubaimed.com/media-center/dubimed-introduces-skinpen-precision-by-crown-aesthetics - **Category:** news - **Published:** 2024-04-01 SkinPen Precision, engineered in the USA, has garnered FDA clearance in 2018 and boasts over 90 validation studies. It is a state-of-the-art skin remodeling device designed for various aesthetic and medical purposes. ### DUBIMED X Dubai Derma 2024 **URL:** https://dubaimed.com/media-center/dubimed-dubai-derma-2024 - **Category:** events - **Published:** 2024-03-13 The event served as a platform for Dubimed to showcase its cutting-edge innovations and engage with industry professionals. Over three eventful three days, Dubimed left an indelible mark on Dubai Derma 2024 with its groundbreaking products and enriching experiences. ### DUBIMED X EPSS 2024 **URL:** https://dubaimed.com/media-center/dubimed-epss-2024 - **Category:** events - **Published:** 2024-01-01 DUBIMED attended the Emirates Plastic Surgery Society (EPSS) meeting held on January 19, 2024. The EPSS is a leading non-profit medical society dedicated to advancing the field of plastic surgery and ensuring patient safety. ### DUBIMED X SkinPen | FDA-Cleared micro-needling **URL:** https://dubaimed.com/media-center/dubimed-skinpen-fda-cleared-micro-needling - **Category:** news - **Published:** 2023-11-23 Unveiling a groundbreaking innovation in skincare, DUBIMED proudly presents SkinPen Micro-needling, a revolutionary FDA-cleared product that will redefine your beauty regimen. ### DUBIMED X Mesoestatic (Cosmelan & Dermamelan) **URL:** https://dubaimed.com/media-center/dubimed-mesoestetic - **Category:** news - **Published:** 2023-11-14 DUBIMED unveils the mesoestetic depigmentation treatments Cosmelan and Dermamelan at the DIAD-DIAL Conference, offering groundbreaking solutions to combat hyperpigmentation and revitalize skin. ### DUBIMED X DIAD-DIAL 2023 **URL:** https://dubaimed.com/media-center/dubimed-diad-dial-2023 - **Category:** events - **Published:** 2023-11-01 We were proud to support the 5th UAE DIAD-DIAL Conference as a Silver Sponsor which starts November 3th 2023 and lasts for 3 days, till November 5th. This premier dual event brought together dermatology and dermatopathology specialists under one roof to exchange knowledge. ### DUBIMED x MEIDAM Conference 2023 **URL:** https://dubaimed.com/media-center/dubimed-meidam-conference-2023 - **Category:** events - **Published:** 2023-09-01 DUBIMED participation MEIDAM Conference 2023, the 8th Middle East International Dermatology & Aesthetic Medicine Conference & Exhibition. ### Sofwave | Clinical Training & Treatment **URL:** https://dubaimed.com/media-center/sofwave-superb-clinical-training - **Category:** news - **Published:** 2023-08-15 Sofwave’s clinical training program equips healthcare professionals with rigorous safety and efficacy techniques for non invasive aesthetic treatments, highlighting how its game changing ultrasound technology ensures optimal results. ### Cellulite Treatment by Sofwave SUPERB Technology: FDA Clearance **URL:** https://dubaimed.com/media-center/cellulite-treatment-by-sofwave-superb-technology-fda-clearance - **Category:** news - **Published:** 2023-08-08 Sofwave’s SUPERB technology has received FDA clearance for improving the appearance of cellulite, offering a non-invasive and effective treatment in a market projected to grow significantly. ### galderma-exclusive-distributor **URL:** https://dubaimed.com/media-center/galderma-exclusive-distributor - **Category:** news - **Published:** 2023-02-01 Galderma Exclusive Dealership by DUBIMED in UAE: The Best in Aesthetic Solutions ### Sofwave™ SUPERB™ Ultimate Non invasive Skin Tightening Solution **URL:** https://dubaimed.com/media-center/sofwave-ultimate-non-invasive-skin-tightening - **Category:** news - **Published:** 2023-01-31 - **Tags:** FDA Approved, ultrasound technology, submental, sofwave, reducing fine lines & wrinkles, neck lifting Introducing DUBIMED’s latest brand Sofwave™ SUPERB™, an FDA‑cleared non‑invasive skin tightening solution utilizing synchronous ultrasound parallel beam technology to stimulate collagen growth, providing effective lifting and tightening results. ### Introducing AnteAGE MDX: The Real Exosomes **URL:** https://dubaimed.com/media-center/introducing-anteage-mdx-the-real-exosomes - **Category:** events - **Published:** 2023-01-05 [roduct launching event for AnteAGE MDX, a cutting-edge skincare solution that promises to revolutionize the beauty industry. ### DUBIMED Kids Academy Season 2 **URL:** https://dubaimed.com/media-center/dubimed-kids-academy-season-2 - **Category:** events - **Published:** 2022-12-14 - **Tags:** Kids Academy, Kids Academy Season 2, DUBIMED CSR DUBIMED Kids Academy Season 2 brought children into real medical environments through hands-on science education, inspiring curiosity, confidence, and future healthcare ambition. ### DUBIMED ISO Certified **URL:** https://dubaimed.com/media-center/dubimed-iso-certified - **Category:** news - **Published:** 2022-11-30 DUBIMED has achieved ISO 9001 certification, demonstrating its commitment to quality management and customer satisfaction. It assures customers of high-quality products and services and signals a step toward leadership. ### DUBIMED Kids Academy Season 1 **URL:** https://dubaimed.com/media-center/dubimed-kids-academy-season-1 - **Category:** events - **Published:** 2020-12-10 - **Tags:** Kids Academy, Kids Academy Season 1, DUBIMED CSR DUBIMED Kids Academy Season 1 brought medical education to life for Dubai's youth. Discover how we're inspiring the next generation of healthcare professionals through hands-on learning and expert instruction. ### MEIDAM CONFERENCE & EXHIBITION 2017 **URL:** https://dubaimed.com/media-center/meidam-conference-and-exhibition-2017 - **Category:** events - **Published:** 2017-09-01 DUBIMED at MEIDAM Conference & Exhibition 2017: Advancing the Field of Dermatology and Aesthetic Medicine in the Middle East --- ## Company knowledge ### DubiMed – Who We Are - **Type:** company_overview - **Audience:** clinics, hospitals, aesthetic centers, dermatologists, plastic surgeons, general practitioners, clinic owners, procurement managers DubiMed is a Dubai-based healthcare company specializing in medical devices, equipment, and aesthetic pharmaceutical (soft) products. We serve clinics, hospitals, and aesthetic centers across the UAE and wider MENA region with cutting-edge solutions and full after-sales support. ## About DubiMed DubiMed is a premier healthcare distribution and solutions company headquartered in Dubai, UAE. We bridge the gap between world-class manufacturers and healthcare professionals by supplying high-quality medical devices, equipment, and aesthetic pharmaceutical products. Our team of specialists ensures every client receives tailored consultation, reliable products, and continuous technical support. --- ## Our Products ### Medical Devices & Equipment - **Diagnostic Equipment** – Patient monitors, ECG machines, ultrasound systems, pulse oximeters, and vital signs monitors - **Surgical Instruments & Tools** – Sterile surgical kits, laparoscopic instruments, electrosurgical units, and suction devices - **Imaging & Radiology** – Digital X-ray systems, portable ultrasound devices, and PACS-compatible imaging solutions - **Intensive Care & Emergency** – Ventilators, defibrillators, infusion pumps, and patient warming systems - **Rehabilitation & Physiotherapy** – TENS/EMS units, ultrasound therapy devices, and hydrotherapy equipment - **Dental Equipment** – Dental chairs, intraoral cameras, digital X-ray sensors, and autoclave sterilizers - **Ophthalmic Devices** – Slit lamps, tonometers, fundus cameras, and auto-refractometers - **Laboratory Equipment** – Hematology analyzers, biochemistry analyzers, centrifuges, and microscopes - **Hospital Furniture & Infrastructure** – Adjustable hospital beds, IV stands, surgical lights, and operating tables - **Sterilization & Infection Control** – Autoclaves, UV sterilizers, and disinfection systems ### Aesthetic & Soft Pharmaceutical Products - **Dermal Fillers** – Hyaluronic acid-based fillers for lip augmentation, facial contouring, and wrinkle correction - **Botulinum Toxin (Botox)** – Certified botulinum toxin products for facial line relaxation and hyperhidrosis treatment - **Skin Boosters** – Injectable hydration treatments for skin rejuvenation and glow enhancement - **Mesotherapy Solutions** – Cocktail injectables for hair loss, skin brightening, and body contouring - **Thread Lift Products** – PDO and PLLA mono, screw, and barbed threads for non-surgical facelifts - **Chemical Peels** – TCA, glycolic acid, salicylic acid, and Jessner peels for professional clinic use - **PRP & Growth Factor Kits** – Platelet-rich plasma kits for facial rejuvenation and hair restoration - **Lipolytic Injectables** – Fat-dissolving solutions for body sculpting and double chin reduction - **Aesthetic Lasers & Energy Devices** – Q-switched lasers, fractional CO2, IPL systems, HIFU, and RF devices - **Microneedling Devices & Serums** – Derma pens and sterile needle cartridges with active serum sets - **Sunscreens & Post-Procedure Skincare** – SPF formulations, calming serums, and recovery creams for clinic retail - **Numbing & Topical Anesthetics** – Lidocaine-based creams and gels for pre-procedure pain management --- ## Our Services - **Product Consultation & Demo** – On-site demonstrations and clinical trials for devices before purchase - **Import & Regulatory Clearance Support** – Assistance with UAE MOHAP and Dubai Health Authority (DHA) product registration - **Installation & Commissioning** – Professional setup and calibration of all medical and aesthetic equipment - **Training & Clinical Education** – Hands-on training sessions for doctors, nurses, and clinic staff on device operation and product application - **After-Sales Technical Support** – Dedicated service engineers providing maintenance, calibration, and spare parts - **Warranty Management** – Comprehensive warranty programs and extended service contracts - **Aesthetic Clinic Setup Consultation** – End-to-end advisory for new clinic launches including equipment selection and layout planning - **Product Distribution & Logistics** – Fast and compliant delivery across UAE with cold-chain capabilities for pharmaceutical products - **Stock Management Solutions** – Consignment and managed inventory options for high-volume clinic partners - **Conference & Workshop Participation** – Regular participation in regional medical and aesthetic conferences for product launches and live demonstrations --- ## Why Choose DubiMed - Licensed and regulated supplier in the UAE - Exclusive regional partnerships with internationally certified brands - Bilingual (Arabic & English) sales and support team - Fast delivery and in-stock availability across product lines - Dedicated account managers for every clinic and hospital partner **Keywords:** medical devices, aesthetic products, dermal fillers, botox, surgical equipment, diagnostic devices, skin boosters, mesotherapy, thread lift, PDO threads, chemical peels, PRP kits, lipolytic injections, aesthetic lasers, HIFU, microneedling, hospital equipment, dental equipment, ophthalmic devices, lab equipment, sterilization, ventilators, ultrasound, ECG, CO2 laser, IPL, RF devices, hyaluronic acid ### DUBIMED Business Model - **Type:** company - **Audience:** both How DUBIMED operates as a distributor and support partner for clinics and healthcare professionals. DUBIMED operates as a specialized distributor and support partner, not as a direct treatment provider. Its model is built around supplying clinics and medical professionals with devices, regenerative solutions, injectables, skincare lines, and related practice support. The company combines product distribution with operational enablement, including installation, training, biomedical support, marketing support, and logistics. This means DUBIMED’s role is not limited to delivering equipment, but also helping clinics launch, operate, maintain, and promote treatments safely and effectively. The company emphasizes authorized distribution, manufacturer-backed partnerships, quality compliance, and regional service coverage as core pillars of its business model. **Keywords:** business model, distribution model, clinic support, medical supply model, authorized distributor ### Marketing Support for Clinics - **Type:** service - **Audience:** b2b Strategic marketing support designed to help aesthetic clinics grow demand, strengthen positioning, and launch treatments more effectively. DUBIMED provides structured marketing support for aesthetic clinics and medical practices across Dubai, the UAE, Qatar, Oman, Saudi Arabia, and the wider GCC region. Its approach combines strategic planning, market understanding, brand visibility work, patient education, campaign support, and launch enablement for new technologies. The company describes its marketing model as a B2C2B approach, where consumer awareness and patient demand generation are developed alongside relationship-building with physicians and referring professionals. Support areas include digital marketing, social media content, branding assistance, promotional concepts, open days, workshops, PR exposure, collaborations, educational content production, event support, and go-to-market planning for technologies introduced into clinics. The service is designed to help clinics improve awareness, reach the right audience, and support sustainable treatment adoption. **Keywords:** marketing support, clinic growth, digital marketing, social media, branding, patient education, campaign launch, b2c2b ### Biomedical Engineering Service - **Type:** service - **Audience:** b2b Technical support, maintenance, installation, and repair for aesthetic medical equipment. DUBIMED provides biomedical engineering support for aesthetic devices and related clinic equipment across Dubai, the UAE, and the GCC. The service covers installation, calibration, preventive maintenance, routine maintenance, emergency service visits, repair coordination, and rapid technical response. The website highlights planned maintenance programs that maximize uptime, extend equipment lifespan, and reduce costly breakdowns. It also emphasizes regular servicing for stable performance, compliance with safety standards, and operational reliability. Emergency support is positioned as a fast-response service intended to restore functionality quickly and reduce disruption to clinic operations. DUBIMED also states same-day response availability in Dubai and 24 to 48 hour coverage across GCC markets depending on the region and service model. This service is part of the company’s promise to remain a long-term technical partner, not only a distributor. **Keywords:** biomedical service, maintenance, installation, repair, preventive maintenance, technical support, calibration, emergency service ### Clinical Training Programs - **Type:** service - **Audience:** b2b Structured training programs for doctors, nurses, and clinic staff using aesthetic technologies. DUBIMED provides clinical training programs for physicians, nurses, and clinic teams working with aesthetic devices and treatments. The training scope includes ultrasound and HIFU technologies, RF microneedling, injectables, body contouring, regenerative medicine, and other device categories used in aesthetic practice. The company describes its training structure as progressing from foundational modules to advanced levels, with a cloud-based learning hub, downloadable guides, recorded sessions, live webinars, flexible demos, live on-site sessions, progress tracking, and ongoing updates on clinical protocols and treatment parameters. Training is positioned as both educational and operational, helping clinics onboard teams, improve confidence, refine technique, and support safe treatment delivery. DUBIMED also presents regional training coverage across Dubai, the UAE, Qatar, Oman, Saudi Arabia, and wider GCC markets through in-person and virtual formats. **Keywords:** clinical training, hands-on training, device training, certification, workshops, live demos, protocol updates, online learning ### Logistics and Distribution Network - **Type:** service - **Audience:** b2b Regional logistics and delivery infrastructure for medical devices, injectables, and clinic supplies. DUBIMED operates a logistics and distribution network built for the handling requirements of aesthetic medical technologies and clinic supplies across the UAE and GCC. The company states that it manages more than 10,000 annual deliveries with a 99 percent on-time delivery rate. The service includes secure warehousing, GPS-tracked fleet operations, WHO GDP-compliant cold chain handling, 24/7 temperature monitoring, FEFO-based inventory control, automated stock monitoring, order accuracy systems, and quality and risk compliance measures. Specialized handling is described for different product categories: large equipment and devices require protective packaging, crating, transport coordination, and support during delivery and positioning; injectable products require refrigerated storage and monitored transport; and consumables require efficient pick-and-pack operations and recurring supply support. The logistics model is presented as a critical part of service continuity for clinics across Dubai, the UAE, Qatar, Oman, Saudi Arabia, and the wider Gulf region. **Keywords:** logistics, distribution, delivery, cold chain, inventory control, gdp compliance, medical supply chain, device transport