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Ellansé S is an injectable dermal filler that combines the benefits of both immediate corrections of lines and wrinkles as well as stimulating the production of the body’s own natural collagen. This combination ensures longer-lasting results and a more youthful and fresh appearance. Ellansé S is to be injected into the mid-deep layer of the skin dermis.
€241.00
Product Information
Active substances | POLYCAPROLACTONE MICROSPHERES, CARBOXYMETHYLCELLULOSE |
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Manufacturer | Sinclair |
Pack size | 2 x 1ml Pre-Filled Syringes |
Strength | 30%, 70% |
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ELLANSÉ™ S represents an innovative advancement in dermal filler technology, combining immediate volumizing effects with long-term collagen biostimulation. This advanced dermal filler utilizes polycaprolactone microspheres suspended in a carboxymethylcellulose gel carrier to deliver dual-action treatment for facial volume restoration and skin rejuvenation.
Medical professionals seeking to purchase ELLANSÉ S will find that this product offers superior longevity compared to traditional fillers, with results lasting approximately 12 months.
Professional administration of ELLANSÉ™ requires proper injection technique using 27G needles at mid-to-deep dermal depths. Each treatment session typically utilizes 1-2 ml of product, depending on the target area and desired correction level. The pre-filled syringe design ensures sterile, precise delivery while maintaining product integrity.
Medical professionals must follow strict aseptic protocols during administration. The injection technique involves slow, controlled delivery with gentle massage to ensure optimal product distribution and dispersion. Treatment duration typically ranges from 30 to 60 minutes, depending on the areas being addressed and the complexity of the correction required.
The core composition of ELLANSÉ™ S consists of polycaprolactone microspheres (30%) suspended in a carboxymethylcellulose gel carrier (70%). These smooth, spherical microspheres measure 25-50 microns in diameter, providing optimal biocompatibility and ELLANSÉ™ S collagen stimulation properties. Additional components include phosphate-buffered saline and glycerin, all of which meet pharmaceutical grade standards.
The synthetic, non-animal-derived formulation eliminates cross-species contamination risks and reduces the potential for allergic reactions. All ingredients undergo rigorous quality control testing to ensure compliance with safety and efficacy standards.
Proper storage requires maintaining temperatures between 15°C to 25°C in controlled environments. Products must be protected from direct sunlight, freezing temperatures, and excessive heat exposure. The sterile packaging should remain intact until immediately before use, and any damaged syringes should be discarded.
Treatment contraindications include active skin infections, inflammatory conditions, autoimmune disorders, and pregnancy or breastfeeding. Patients with a tendency to form keloids or those with skin hypersensitivity require careful evaluation before treatment. Previous adverse reactions to similar fillers represent absolute contraindications.
A medical history assessment must identify any concurrent medications that may increase the risk of bleeding or interfere with the healing process. Practitioners should exercise clinical judgment when evaluating patients with compromised immune systems or ongoing medical treatments.
Healthcare providers must possess the appropriate training and licensing for administering dermal fillers. Proper injection technique is essential to avoid vascular complications, nerve damage, or unintended product placement. Emergency protocols should be established for managing adverse events.
Patients require comprehensive consultation regarding realistic expectations, potential risks, and post-treatment care requirements. The irreversible nature of ELLANSÉ™ filler necessitates careful treatment planning and conservative initial volume correction approaches.
AQTIS Medical BV manufactures ELLANSÉ™ products under ISO 13485 certification in the Netherlands. The product maintains CE-marking for European distribution and complies with Class III medical device regulations. Regulatory approval ensures safety and efficacy standards for professional dermal treatment applications.
Healthcare professionals can buy authentic products through licensed distributors who provide verification of lot numbers and manufacturing dates. When medical practices order ELLANSÉ™ fillers, they receive comprehensive documentation supporting regulatory compliance and professional liability requirements.
ELLANSÉ™ S is specifically designed for facial volume restoration and soft tissue augmentation in adult patients. The product addresses multiple aesthetic concerns, including nasolabial folds, marionette lines, loss of cheek volume, and facial contouring needs. Licensed medical professionals can utilize this filler for comprehensive facial rejuvenation treatments that provide both immediate and progressive improvements.
The primary advantage of ELLANSÉ™ S lies in its innovative dual-action mechanism that delivers immediate volume correction while stimulating natural collagen production over time. This approach provides patients with instant gratification and progressive improvement, resulting in long-lasting results that can extend up to 12 months.
Common side effects include temporary swelling, redness, bruising, and tenderness at injection sites, typically resolving within 24-48 hours. These results reflect normal tissue response to injection procedures and generally do not require specific intervention beyond standard post-treatment care.
Rare complications may include skin necrosis, facial asymmetry, or granuloma formation. Immediate medical attention is required for severe reactions including persistent pain, vision changes, or signs of vascular compromise.
Kinami Health prides itself on supplying genuine, high-quality medical injectables and supplies to hospitals, medical clinics, and licensed medical professionals around the world.
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Contact
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Triq Id-Dejqa, Valletta, VLT 1431, Malta
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