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| Active substances | CROSS-LINKED HYALURONIC ACID (HA), MANNITOL |
|---|---|
| Manufacturer | Vivacy |
| Pack size | 2 x 1ml Pre-Filled Syringes, 4 x 30G ½ Needles |
| Strength | 24mg/g HA, 9mg/ml Mannitol |
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STYLAGE® L BI-FLEX® is used for the correction of deep to very deep wrinkles, facial folds, and volume-related concerns. It is especially suitable for areas where a denser hyaluronic acid gel is required to support visible smoothing and contour correction.
Key benefits include:
Results may vary depending on the patient’s skin condition, age, treatment area, injection technique, and individual metabolism. No aesthetic outcome should be presented as guaranteed.
STYLAGE® L BI-FLEX® is formulated with cross-linked hyaluronic acid, designed to provide filling, smoothing, and volumizing support in professional aesthetic treatments.
The formula also contains mannitol, an antioxidant included to help protect the hyaluronic acid gel from oxidative stress. This supports product stability and contributes to the performance of the filler during treatment.
STYLAGE® L BI-FLEX® is designed for professional use and should only be handled by trained medical or aesthetic practitioners familiar with dermal filler injection protocols.
Each pack of STYLAGE® L BI-FLEX® typically includes:
Additional clinical materials may be required depending on the practitioner’s preferred technique, treatment area, and clinic protocol.
STYLAGE® L BI-FLEX® should be stored according to the manufacturer’s instructions and kept in its original packaging until use. Protect the product from direct sunlight, freezing, contamination, or improper handling.
Clinics should always check the expiry date, packaging integrity, batch number, and storage conditions before administration.
STYLAGE® L BI-FLEX® is administered by injection into the appropriate dermal layer depending on the treatment indication, patient anatomy, and desired correction. Common techniques may include linear threading, serial puncture, fanning, or cross-hatching, depending on the treatment area.
This product must only be injected by licensed and trained healthcare professionals with knowledge of facial anatomy, dermal filler safety, and complication management.
After treatment, patients should follow the practitioner’s post-care instructions. General recommendations may include avoiding excessive pressure on the treated area, intense exercise, alcohol, saunas, sunbeds, and extreme heat or cold for the first 24–48 hours.
Patients should be advised not to massage or manipulate the treated area unless specifically instructed by the practitioner.
Possible side effects may include temporary redness, swelling, bruising, tenderness, itching, firmness, or mild discomfort at the injection site. These reactions are usually short-term and related to the injection procedure.
Less common complications may include nodules, infection, inflammation, allergic-type reactions, vascular complications, or uneven results. Any unusual or persistent symptoms should be assessed by a qualified healthcare professional.
STYLAGE® L BI-FLEX® should not be used in patients with known hypersensitivity to any ingredient, active skin infection, inflammation in the treatment area, or a history of severe allergic reactions.
Treatment may not be suitable during pregnancy or breastfeeding, or for patients with certain autoimmune conditions, bleeding disorders, or those using anticoagulant medication. A full medical consultation should always be completed before treatment.