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ART FILLER VOLUME

Availability: Available
Brand: Art Filler
Typologies: Filler

128,50

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VOLUME is an injectable implant indicated for restoring volume to the mid-facial area, temples, jaw and chin, by subcutaneous, supraperiosteal or deep dermal injections. The presence of lidocaine is intended to reduce pain sensations in the patient during treatment.
USE MEDICAL STRICT. Medical device. Injection of hyaluronic acid. Use reserved for dermatologists and aesthetic doctors because they require a medical procedure.

 

 

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VOLUME is an injectable, resorbable gel:
- Viscoelastic based on cross-linked hyaluronic acid of non-animal origin.
- Colourless, transparent, sterile, apyrogenic and physiological.
- Containing 0.3 % by mass of lidocaine hydrochloride for its anaesthetising properties.
- Tri Hyal® Technology.

- FILLMED LABORATOIRES
- NAME: VOLUME
- COMPOSITION: Cross-linked hyaluronic acid 25 mg, lidocaine hydrochloride 3 mg, phosphate buffer pH 7.2 QSP 1 g.
- PRESENTATION: 2 x 1.2ml.
- INDICATIONS: VOLUME promotes perfect integration of the product in the tissues, helping to restore the natural volumes of the face. It is indicated for reconstructing emptied areas and filling in the deepest skin depressions, restoring harmony and proportion to the features. The formula combines three types of hyaluronic acid, which act in synergy to offer three complementary corrective actions, redefining facial contours, restoring natural fullness and lifting the skin's surface.
- INJECTION DEPTH: Subcutaneous, supraperiosteal or deep dermal injections.
- NEEDLES: 4 x 27G½”.
- DURATION: Clinically significant improvement 18 months after treatment.
- USE: Strict medical use.

- Syringes: 2 x 1.2 ml.
- Needles: 4 x 27G½”.
- Each box contains two single-use pre-filled syringes of 1.2mL VOLUME and 4 sterile 27G½” disposable needles reserved for VOLUME injection, a package insert and 4 traceability labels.

Face, temples, jaw and chin.

Cross-linked hyaluronic acid 25 mg, lidocaine hydrochloride 3 mg, phosphate buffer pH 7.2 QSP 1 g.

The use of VOLUME is reserved for doctors trained in injection techniques.
No clinical data are available on the efficacy and tolerance of injecting VOLUME into an area previously treated with another filler product.
No clinical data are available on the efficacy and tolerance of VOLUME injection for Fitzpatrick phototypes V and VI.
No clinical data are available on the efficacy and tolerance of VOLUME injection in patients with a history of multiple severe allergies or anaphylactic shock. The doctor must therefore decide on a case-by-case basis on the indication depending on the nature of the allergy and must ensure special monitoring of such patients at risk. In particular, it may be decided to propose a double test or a suitable preventive treatment before any injection.
VOLUME should be used with caution in patients with cardiac conduction disorders.
VOLUME should be used with the utmost caution in patients with hepatocellular insufficiency with coagulation disorders, as well as in patients treated with drugs that reduce or inhibit hepatic metabolism and could therefore cause coagulation disorders.
The injection volume depends on the level of correction required and is at the doctor's discretion. The recommended dose per treatment site is 1.2 ml. A maximum of two treatment sessions per year is recommended. Possible touch-up sessions allow the desired level of correction to be maintained. The maximum recommended dose per year is 15 ml.
Patients should receive the following recommendations:
- Avoid taking aspirin, high-dose vitamin C and/or E in the week before the injection.
- Patients undergoing anticoagulant treatment should be warned of the increased risk of bruising and bleeding during injection.
- Do not apply make-up for 12 hours after the injection.
- Avoid exposure to extreme temperatures (intense cold, sauna, Turkish bath), as well as prolonged exposure to the sun and ultraviolet rays for 2 weeks after the injection.
If the needle is obstructed, do not increase the pressure on the piston rod but stop injection and replace the needle.
The physician's attention is drawn to the fact that this product contains lidocaine and should therefore be duly taken into account.
Athletes' attention is drawn to the fact that this product contains an active ingredient that may induce a positive reaction in doping tests.

VOLUME must not be injected:
- For the correction of superficial wrinkles.
- In the periorbital (eyelid, crow's feet, dark circles) and glabellar region nor in the lips.
- In the blood vessels .
- In the muscles.
- In a site where a non-absorbable filler implant has already been injected.
- Do not over-correct.
VOLUME must not be used:
- In patients with known hypersensitivity to hyaluronic acid, lidocaine and amide-type local anaesthetics.
- In patients with a history of auto-immune disease or undergoing immunotherapy.
- In patients with epilepsy that is not controlled by treatment.
- In patients with porphyria.
- In patients with a tendency to develop hypertrophic scars.
- In patients with a history of relapsing angina associated with acute joint rheumatism with cardiac localisation.
- In pregnant or breastfeeding women.
- In children.
- In areas with inflammatory and/or infected skin lesions (acne, herpes, etc.).
- In direct association with a treatment by laser, deep chemical peeling or dermabrasion.

VOLUME with Tri-Hyal Texture Technology, is an easy-to-mould filler indicated for volume and facial contours.

The contents of VOLUME syringes are sterilised by moist heat. The 27G½” needles are sterilised by irradiation.

INCOMPATIBILITY
There are incompatibilities between hyaluronic acid and quaternary ammonium compounds such as benzalkonium chloride solutions. VOLUME must therefore never come into contact with medical/surgical instruments treated with this type of product.

FAQ

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VOLUME is indicated for restoring volume in the mid-facial area, temples, jaw and chin, by subcutaneous, supraperiosteal or deep dermal injections. It is not indicated for lips, eyelids, superficial wrinkles or periocular areas.

Tri-Hyal Technology combines three types of cross-linked hyaluronic acid, which work in synergy to offer three corrective actions: redefining contours, restoring natural fullness and lifting the skin's surface.

Clinically significant improvement can last up to 18 months, with the possibility of touch-up sessions as assessed by the physician. The maximum recommended dose per year is 15 ml.

The product is contraindicated in patients with an allergy to hyaluronic acid or lidocaine, active autoimmune diseases, uncontrolled epilepsy, porphyria, pregnant or breastfeeding women, children, or in skin areas that are inflamed or treated with deep peeling, laser or dermabrasion.

It is recommended to avoid anticoagulant drugs or high-dose vitamins C and E in the week before the injection, not to apply make-up for 12 hours after the injection, and to limit exposure to sun, intense cold, sauna or steam baths for 2 weeks afterwards. Patients should also follow the doctor's instructions for any touch-ups.

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