HYACORP BODY CONTOURING MLF 1 is a sterile, non-pyrogenic, viscoelastic, biocompatible (non-immunizing, insensitive, non-toxic) gel implant that does not dissolve in water and is derived from hyaluronic acid obtained by fermentation. Hyaluronic acid is a natural polysaccharide in the dermal matrix of human skin. Hyaluronic acid in the tissues of all higher organisms is chemically, physically and biologically identical.
HYACORP BODY CONTOURING MLF1 has the following elements in solution (per 1 ml):
- Hyaluronic acid 2.0 mg
- Hyaluronic acid crosslinked with 20.0 mg
- Sodium chloride 6.9 mg
- Water for Injection 1.0 ml.
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HYACORP BODY CONTOURING MLF1 is implanted in the subcutaneous and/or super-periosteal tissue to complement the intercellular matrix and intradermal tissue to restore lost anatomical structures. Its mechanism of action is based on the latest biotechnological developments in the field of injection agents, based on hyaluronic acid. The effects of the product will be shown in some time.
The areas to be treated must be marked before treatment begins. A local anaesthetic can be administered in order to carry out the implant as painlessly as possible. An antibiotic can be administered at the doctor’s discretion to prevent infection. Remove the syringe from the blister pack, remove the cap covering the tip of the syringe and fit a suitable sterile needle to the Luer Lock port.
The implantation technique in terms of the depth of the injection and the amount administered can vary from case to case and according to the different degrees of augmentation required. The doctor must select the technique appropriate to the case in hand. Correct only up to 100 % of the volume of augmentation required. Do not carry out overcorrections. Explanations must be given to the patient before treatment is given about indications, warnings, intolerances as well as potential side effects and the results to be expected. The area to be
treated must be carefully aseptically prepared before treatment.
The graduation on the syringe is intended as a guide for users based on the final volume. It does not perform any measuring function; it merely indicates the amount used in relation to the nominal volume of 10 ml. The doctor administering treatment should check visually and by touch that a sufficient amount of the material has been injected.
The product must not be resterilised. It must not be mixed with other injection materials or decanted. The product must not be used if the packaging and the blister pack are damaged.
Do not freeze or expose to extreme heat. Store at room temperature
(2 °C – 25 °C).
BioScience GmbH