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Ellansé M (2x1ml)
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zł1,498.00
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The lowest price of the product zł749.00 in day 02.01.2026
Ellansé M is a sterile, apyrogenic, fully absorbable subcutaneous implant, classified as a tissue stimulator with a prolonged duration of action. It consists of synthetic polycaprolactone (PCL) microspheres suspended in a carboxymethylcellulose (CMC) based gel carrier. The device exhibits a dual-phase mechanism of action: immediate mechanical correction and secondary induction of neocollagenesis.
mechanism of action
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initial phase (mechanical correction): The CMC gel carrier (70% by volume) provides immediate interstitial filling and mechanical correction of volume deficits directly after injection
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stimulation phase (neocollagenesis): The PCL microspheres (30% by volume, size 25-50 microns) act as a scaffold for fibroblasts, inducing the production of endogenous Type I collagen. This process allows for the restoration of the extracellular matrix (ECM) structure and long-term improvement of the skin's biomechanical parameters
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bioresorption: The implant undergoes complete degradation into water and carbon dioxide (via the Krebs cycle), ensuring long-term safety
indications and intended use
The device is intended for administration via injection by authorized medical personnel to:
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correction of volume deficits: fill nasolabial folds, marionette lines, and atrophic scars
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facial contour modeling: improve the projection of cheeks, jawline, and temples
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structural wrinkle reduction: reduce forehead and perioral wrinkles
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tissue biostimulation: restore density and elasticity to skin affected by the aging process
injection technique
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depth: subcutaneous layer or deep layers of the dermis
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technique: linear-retrograde (stringing), fanning technique
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tools: recommended 27G 20mm needle or cannula (depending on the area)
composition
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Polycaprolactone (PCL) microspheres: 30% (stimulating spheres)
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Carboxymethylcellulose (CMC) gel carrier: 70% (USP carrier)
contraindications
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pregnancy and lactation
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active autoimmune diseases, uncontrolled diabetes, history of neoplastic disease
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viral, bacterial, or inflammatory infections in the treatment area
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known hypersensitivity to any component of the preparation
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presence of permanent fillers in the planned injection area
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use of anticoagulants (relative contraindication)
post-treatment recommendations
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do not massage or press the injection area for at least 24 hours (unless otherwise directed by a physician)
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avoid extreme temperatures (sauna, solarium, sun exposure) and use SPF 50+ photoprotection for a period of 14 days
duration of effect
- up to 24 months (depending on the product variant and individual patient characteristics)
contents
- 2 pre-filled syringes (1 ml each)
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PRE-FILLED SYRINGE |
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The product may only be used by professionals. By making a purchase, you declare that you are a doctor or cosmetologist trained in aesthetic medicine. |
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