RAPID DISPATCH
24/H dispatch
2 in stock
MD-MATRIX is a collagen-based medical device designed to aid movement by limiting physiological degeneration of joints and tissues.
USE MEDICAL STRICT. Medical device. Use reserved for dermatologists and aesthetic doctors because they require a medical procedure.
MD-MATRIX is an injectable class III medical device:
- It improves movement.
- It helps contain the physiological deterioration of connective tissue and extracellular matrix.
- It can be combined with other types of treatment.
- GUNA S.P.A.
- NAME: MD-MATRIX
- COMPOSITION: Collagen of porcine origin, Citric acid, Nicotinamide, Sodium chloride, Water for injection.
- PRESENTATION: 10 x 2ml.
- INDICATIONS: Strengthens the extracellular matrix of connective tissue.
- INJECTION DEPTH: Peri-articular, intradermal and/or subcutaneous.
- PROTOCOL: 1-2 infiltrations per week to limit the physiological deterioration of joints and tissues (tendons and ligaments). Results are evident from the third or fifth week.
- USE: Strict medical use.
- Vials: 10 x 2ml.
Thighs, knees, abdominal area, hips, buttocks and arms.
Collagen of porcine origin, Citric acid, Nicotinamide, Sodium chloride, Water for injection.
- The product is only to be used by qualified healthcare professionals in suitable facilities using the injection technique: appropriate site, disinfection, sterile instruments.
- Ensure that the seal on the vial has not been tampered with and that the packaging is intact.
- Store the product under appropriate conditions (temperature indicated, protection from light and frost) as indicated by the manufacturer.
- After opening the vial, use it immediately. Do not store unused contents for an extended period of time.
- If there are skin lesions, infections or heavily inflamed areas at the injection site, carefully evaluate the procedure or postpone: the area must be prepared aseptically.
- Check that the patient is not already known to be hypersensitive to collagen of porcine origin or other components of the product.
- Inject with appropriate technique (needle profile, depth, volume, mode) according to the indicated protocol and in agreement with the patient.
- Inform the patient about possible local reactions (e.g. redness, slight pain/burning at the injection site), which usually resolve within a short time.
- Keep the product out of the reach of children and under medical supervision.
- Do not use the product after the expiry date indicated on the packaging.
MD-MATRIX is contraindicated in the following cases:
- There are no documented historical cases of specific hypersensitivity to MD-MATRIX.
- Do not use in patients with known hypersensitivity to one or more components or excipients of the product.
- Since it is an injectable device, the treatment should only be performed by qualified personnel in a suitable healthcare facility.
Aesthetic and regenerative medicine:
To tone the subcutaneous or microvascular connective layer at localised adiposities and fibro-edemo-geloid excess connective layer (thighs and knees).
As a topical treatment, mesotherapy or subcutaneous injection to counteract physiological ageing and other changes in skin and subcutaneous tissues (abdominal area, knees).
Osteo-arthro-myofascial pathologies:
The following associations are clinically documented
with MD-MUSCLE and MD-NEURA for the treatment of facial neuralgia.
with MD-HIP for the treatment of hip arthrosis.
with MD-SHOULDER for the treatment of acute scapulohumeral periarthritis and subdeltoid bursitis.
MD-MATRIX is a collagen-based injectable medical device that helps strengthen the extracellular matrix, improve tissue mobility and slow down physiological degeneration of joints, tendons and ligaments.
The product can be administered via periarticular, intradermal or subcutaneous infiltrations, following a protocol of 1-2 infiltrations per week; results may become visible between the third and fifth week of treatment.
It is indicated for thighs, knees, abdomen, hips, buttocks and arms, both for aesthetic medicine and regenerative support of connective tissues.
There are no documented historical cases of specific hypersensitivity, but it is contraindicated in patients with a known allergy to any of the components, particularly to collagen of porcine origin.
Only qualified medical personnel in suitable medical facilities, as this is an injectable medical device that requires sterile technique and clinical evaluation of the patient.