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Neauvia Organic Stimulate 1 pre-filled syringe of 1ml

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€83.84
€83,840.00/l
From €79.00
Neauvia Organic Stimulate 1 pre-filled syringe of 1ml
Neauvia Organic Stimulate 1 pre-filled syringe of 1ml
Description Our selection Customer reviews

NEAUVIA
Stimulate
26 mg/ml cross-linked Hyaluronic Acid
Glycine and L-Proline
Temporary correction of congenital and acquired soft tissue defects of the Face by intradermal injections
Class III medical device
The box contains a 1ml pre-filled syringe, instructions for use, a needle and a set of labels to identify the product.

NEAUVIA Organic Stimulate is a sterile, non-pyrogenic, non-nonophasic hydrogel for injections. NEACM A Organic Stimulate is made from highly purified sodium hyal uronate, of non-animal origin, obtained from bacterial fermentation, non-pathogenic to Man. NEAUVIA Organic Stimulate is composed of hydroxyapatite microspheres. This hydrogel is gelatinous, semi-transparent and whitish. It comes in 1.0 ml disposable pre-filled syringes with Luer look tips. The box contains a syringe, instructions for use, a needle and a set of labels to identify the product.

NEAUVIA Organic Stimulate is a medical injection product designed to temporarily correct congenital and acquired facial soft tissue defects by intradermal injections. Once injected, this product degrades slowly.

Please note that injecting Neauvia Stimulate requires a medical procedure that can only be carried out by a doctor (a doctor specialising in dermo-aesthetics, a dermatologist or a plastic surgeon).
THE PRODUCTS SOLD ON OUR SITE ARE PARAPHARMACEUTICAL PRODUCTS, SO THEY ARE AVAILABLE OVER THE COUNTER AND DO NOT REQUIRE A PRESCRIPTION.
This is a medical device
This product cannot be returned or exchanged.

REF:
8053736080008

The composition may be subject to variations, so we advise you to always check the list on the purchased product.

Composition: NEAUVIA Organic Stimulate is a cross-linked polymeric hydrogel containing 26 mg/ml of stabilised sodium hyaluronate and hydroxyapatite (1%), Glycine and L-Proline in apymgene buffered water.


CONTRAINDICATIONS:

- Autoimmune skin diseases.
- Infections and inflammations (acne, herpes, dermatitis, etc.) in or near the treatment area.
- Varicose veins in the injection area.
- Patients undergoing treatment with anticoagulants.
- Patients undergoing radiotherapy or ultrasound therapy in the treatment area.
- Patients with a tendency to develop hypertrophic scars. Patients who are hypersensitive to Hyaluronic Acid.
- Patients suffering from untreated epilepsy.
- Pregnant women and milk feeding mothers.
- Children and adolescents under the age of 18.
- Patients with a history of severe allergies.
- Patients who have received other temporary or permanent fillers in the same treatment area.
- Do not inject into the periorbital region (eyelids, dark circles, crow's feet) and the glabellar region.
- Do not inject into blood vessels.
- Do not use excessively.
- Do not use in conjunction with laser therapy, deep chemical peels or dermabrasion.
- Do not inject into the mammary gland or internal genitalia

PRECAUTIONS FOR USE:

This product can only be administered if all the specific conditions are met, in a suitable environment. It should therefore only be used by doctors who have received specialist training in dermal filler injection techniques

WARNINGS:

- Do not use after the expiry date.
- Do not use if packaging is damaged, opened or improperly stored.
- Do not use if the product appears abnormal (see "Description and composition").
- Apply the product immediately after opening the pack; do not store residues.
- Do not inject the product contained in the same syringe into different patients.
- Do not use the same needle for different parts of the Body.
- Do not mix the product with other substances.
- Avoid contact with quaternary ammonium salts such as benzalkonium chloride.
- Do not add medicines to the hydrogel.
- The product is for single use only; re-use may result in loss of sterility and have serious consequences for the patient's health

REACTIONS TO TREATMENT AND ADVERSE REACTIONS:

The doctor must inform the patient of any possible adverse effects associated with the application of the product which may occur immediately or some time after the injection. Following the injection of Hyaluronic Acid some adverse reactions have been noted. These include but are not limited to:
- Inflammatory reactions such as redness, swelling, erythema, etc. which may be accompanied by itching or pain on pressure, or both;
- Ecchymosis/haematomas;
- Spotting and discoloured Skin around the injection site;
- Product intolerance reactions;
- Increased sensitivity at the injection site;
- Infection;
- Unsatisfactory filling effect of the product;
- Appearance of granuloma;
- Dislocation of the product;
- Numbness;
- Grume;
- Necrosis;
- Papules and nodules at the injection site;
- Allergic reactions to one or more of the components of the product. Inform your doctor as soon as possible of any adverse reaction (above or otherwise) lasting more than a week. The implant must be checked and treated appropriately.
The resolution of any adverse event related to the implant is closely linked to the speed of intervention.
Any adverse events associated with treatment using NEAUVIA Organic Stimulate should be reported directly to the manufacturer and/or distributor of the product.

STORAGE
- Storage temperature between 4° C and 27° C.
- Do not expose to direct sunlight.
- Do not freeze or heat.

The manufacturer declines all responsibility for direct, indirect or consequential damage caused by an error in use or abnormal use of the NEAUVIA Organic Intense product or by its use in a manner other than that described in these instructions. The user is responsible for verifying the suitability of the product for the intended use, and therefore assumes all risk and liability in this regard.

DISPOSAL OF THE PRODUCT
To avoid biological risks, handle and dispose of syringes and needles in accordance with health centre procedures and regulations.
The product may only be used by doctors.

These class III medical devices are regulated health products which, under these regulations, carry the CE mark. Manufacturer : MATEX LAB SPA, via Carlo Urbani 2ang. via Enrico Fermi, Brindisi, Italy. Please read the instructions for use carefully. The use of these products requires the intervention of a health professional.

This product is intended for professional use by doctors who choose their own administration technique. However, it is advisable to carry out the implantation according to the manufacturer's injection instructions.


PREPARATION FOR TREATMENT
- Recommended needle: 21 G
- Recommended cannula: 22 G
- The doctor should ask the patient about his or her health history (current infections, medication taken, current dental treatment, surgery, Allegy, etc.).
- Record the REF (type of product) and batch number of the product used in the patient's medical record to ensure traceability.
- Inform the patient of all the indications, contraindications and possible adverse reactions that may be caused by the use of the product.
- Ask the patient to sign an informed consent form.

ANESTHESIA: In order to avoid any allergic reaction, the product does not contain any anaesthetics.
- Assess the need for a local anaesthetic. In this case, the local nerve block technique (truncular) is preferred.
- In the case of a patient suffering from Allegies, assess whether it is appropriate to use an anaesthetic.

PROCEDURE TO BE FOLLOWED FOR TREATMENT
- Before injecting the product, carefully disinfect the area to be treated (povidone iodine or chlorhexidine-based disinfectant).
- Remove the protective cap from the syringe.
- Screw the needle onto the Luer Lock connector on the syringe.
- Gently push the plunger to remove any residual air from the syringe.
- If the needle becomes blocked, do not increase the plunger pressure but replace the needle.
- Inject the product slowly, using the retrograde injection method.
- During injection, the product can be shaped with the other hand.
- After injection, gently massage the treated area to distribute the product.

POST-TREATMENT ADVICE
- The doctor may prescribe anti-inflammatory medication to reduce swelling after the injection, a natural physiological response to any dermal filler injected.
- To reduce any inflammatory effects typically caused by an injection, ice may be applied to the treatment area but not directly to the Skin.
- Bruises/haematomas can be treated with appropriate gels and creams.
- Do not touch the skin or use Cosmetics on the treatment area for 24 hours after administration.
- No surgical or dental procedures should be carried out for a fortnight following the injection. Otherwise, it is essential to ALWAYS inform the doctor concerned of the place where the injection was given.
- Any aesthetic treatment (laser, peelings, etc.) is also not recommended in the treatment area for three weeks after the injection.
- It is recommended to avoid direct exposure to the Sun and UVA-B rays (tanning lamps) for a fortnight after the injection.

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