Aliaxin® LV

Aliaxin® LV

Aliaxin

Medical aesthetic product
  • CE Marked Class III medical device for professional use.
Dermal filler \u2014 hyaluronic acid (lip volume)

Description

Aliaxin® LV Lips Volume is a resorbable, sterile, non-pyrogenic, physiological hyaluronic acid gel filler specifically developed for lip volumisation and contouring, and for correction of medium and deep facial skin sagging. Based on cross-linked, non-animal HA produced by biofermentation, it provides harmonious and natural lip volume, restores firmness and definition, and treats common facial imperfections such as nasolabial folds and perioral wrinkles. The ready-to-use monophasic gel shows high tissue integration and stability, offering long-lasting, natural-looking results.

Bnefits

  • Designed specifically for harmonious increase of lip volume and improved lip contour.
  • Restores lip firmness while maintaining a natural look and feel.
  • Treats medium and deep facial wrinkles and sagging (e.g. nasolabial folds, glabellar and frontal lines).
  • Provides high tissue integration and stability for smooth, natural results and prolonged effect.
  • Ultrapure, non-animal hyaluronic acid produced by patented biofermentation with low BDDE residue and low cross-linking percentage.
  • Monophasic gel, ready to use without additional handling, optimised viscoelastic properties for flow, lift and sculpting.
  • Temporary, fully resorbable filler with typical duration of 6–12 months depending on patient and treatment.

Indications

  • Lip volumisation and contour enhancement.
  • Restoration of physiological facial volumes.
  • Correction of medium and deep sagging skin of the face.
  • Nasolabial folds.
  • Circumoral/perioral wrinkles.
  • Glabellar wrinkles.
  • Frontal (forehead) wrinkles.
  • Facial and acne scars.
  • Areas requiring enrichment of facial tissue (cheeks, chin, cheekbones, lips) with temporary volume increase.

Composition

  • Cross-linked hyaluronic acid (non-animal origin) 25 mg/ml.
  • Natural (non-cross-linked) hyaluronic acid 2.5 mg/ml.
  • Molecular weight fractions: 1000 kDa and 2000 kDa.
  • Phosphate buffer.
  • Water for injectable solutions.
  • Cross-linking agent: BDDE, low percentage cross-linking (<10%) and low BDDE residue (<0.1 ppm).

Formulation

  • Monophasic, sterile, non-pyrogenic, physiological HA gel.
  • Ready-to-use pre-filled syringes; no fragmentation or extra handling required.
  • Rheological profile: Flow 0.53, Lift 39 Pa, Sculpt 0.28.
  • Hydroaction 2/4 and Liftaction 4/5 for combined hydration and lifting performance.

Packaging

  • Total volume: 2 ml (2 × 1 ml pre-filled disposable sterile syringes).
  • 2 sealed blister packs, each containing one single-dose sterile syringe of 1 ml.
  • 4 single-use sterile needles: 27G × 13 mm (½") and 27G × 19 mm (¾").
  • Instruction leaflet (notice).
  • Adhesive labels for patient file and product traceability.

Usage

  • Use exclusively by qualified medical personnel experienced in dermal filler injections.
  • Check integrity of packaging and expiry date; do not use if damaged or expired.
  • Disinfect treatment area and maintain strict aseptic technique.
  • Inject into the skin tissue (mid to deep dermis and/or lip tissue) for extracellular matrix supplementation and intracutaneous volumetric increase.
  • Select injection technique (e.g. linear threading, serial puncture, fanning) according to indication and treatment plan.
  • Adjust injected volume according to degree of correction required and specific treatment area, avoiding overcorrection.
  • After injection, gently massage treated area if needed to ensure even gel distribution.
  • Provide post-treatment advice, including avoiding intense heat/cold, vigorous exercise and manipulation of the lips or treated area for a short period.
  • Single-use device: discard any unused product, syringes and needles as clinical waste.

Contraindications

  • Hypersensitivity to hyaluronic acid or any component of the product.
  • Active skin infection, inflammation or lesions near the intended injection site.
  • Patients with a history of severe allergies or anaphylactic reactions.
  • Pregnancy and breastfeeding (use not recommended).
  • Severe autoimmune or immune system disorders (at physician’s discretion).
  • Individuals under 18 years of age.

Adverse Effects

  • Temporary redness (erythema), swelling, tenderness or pain at the injection site.
  • Bruising or hematoma.
  • Itching or transient discolouration.
  • Palpable nodules or lumps, usually transient.
  • Rare complications such as infection, granuloma formation, vascular occlusion or necrosis if injected intravascularly.
  • Hypersensitivity or allergic reactions in susceptible patients.

Storage Conditions

  • Store at 2–25°C (or 2–28°C as per packaging).
  • Do not freeze.
  • Keep in original packaging and protect from light.
  • Do not use after the expiry date indicated on the pack.

Duration

Typically 6\u201312 months, depending on treated area, degree of correction, patient age, skin type and lifestyle.

Onset

Immediate

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