Description
MD-KNEE
Description
Medical device useful for improving the mobility of the knee joint, whose primary therapeutic treatment consists of the following functions:
1. Barrier effect.
2. Lubricating activity.
3. Mechanical support in case of ongoing drug therapy.
The use of MD-KNEE is recommended by qualified healthcare personnel, in private or public healthcare facilities for:
- improve knee mobility;
- promote muscle relaxation;
- relieve knee pain and projected pain during movement.
How to use
MD-KNEE can be used alone or in combination with other medical devices from the same line, in order to guarantee personalized treatment based on the individual clinical picture.
In cases where supportive treatment is required for the onset of acute pain, MD-KNEE can be combined with MD-NEURAL, MD-POLY and MD-MUSCLE (one or more of these).
Furthermore, in cases where tissue matrix support therapy is required or a slowing down of physiological aging is necessary, MD-KNEE can be combined with MD-MATRIX and MD-TISSUE.
Therapeutic protocol :
1 treatment per week for 10 consecutive weeks.
Method of administration: periarticular injection (the application area must be aseptic; insert the needle to a depth of 2-4 mm).
For this use of the medical device, the use of the following materials and accessories is recommended:
• Material to ensure skin asepsis: disposable glove, iodine-based solution, alcohol solution, sterile gauze, ethyl chloride-based skin spray.
• Needles: sterile 27 G.
• Syringes: 5 or 10 cc, depending on the quantity of solution to be injected.
Method of administration: intra-articular injection.
For this use of the medical device, the use of the following materials and accessories is recommended:
• Material to ensure skin asepsis: disposable glove, iodine-based solution, alcohol solution, sterile gauze, ethyl chloride-based skin spray. The application of local anesthetic on the treated skin is recommended.
• Needles: sterile 22 G.
• Syringes: 2 cc, depending on the quantity of solution to be injected.
Intra-articular injection treatment (inner side) :
The patient lies supine with the knee slightly flexed. Introduce a 22-gauge needle toward the plane of the posterior surface of the patella in the medial and lateral positions.
Components
Collagen of porcine origin.
Excipients: Arnica, NaCl, water for injection.
Warnings
Disposable.
No case of hypersensitivity has been reported.
Contains collagen of animal origin from porcine species. Patients with known hypersensitivity to the component or excipients should be previously subjected to an injection test in the arm and kept under observation for one hour.
Knee pain requires differential diagnosis with damage to the collateral or cruciate ligaments, prepatellar bursitis, painful hip pathologies, osteochondritis dissecans, predominantly inflammatory arthropathy, gout, septic arthritis.
Slight redness at the injection area may be due to the mechanical effect of the needle or a skin reaction.
The application may cause burning/pain symptoms at the injection sites, which generally resolve within 5-10 minutes after the end of treatment.
Skin cleaning/disinfection is required before and after application.
Any pyogenic bacteria may produce an abscess in the injection area.
Keep out of the reach and sight of children.
Do not use after expiration.
Use the product immediately after opening.
Do not use if seal is broken or tampered with.
After opening, the contents of the vial must be injected immediately.
Do not use if packaging is damaged.
Conservation
Store at a temperature between 2°C and 30°C, protect from sunlight and frost.
The expiry date refers to the product in its intact packaging, stored correctly.
Format
Pack of 5 sterile 2 ml vials
Medical device useful for improving the mobility of the knee joint, whose primary therapeutic treatment consists of the following functions:
1. Barrier effect.
2. Lubricating activity.
3. Mechanical support in case of ongoing drug therapy.
The use of MD-KNEE is recommended by qualified healthcare personnel, in private or public healthcare facilities for:
- improve knee mobility;
- promote muscle relaxation;
- relieve knee pain and projected pain during movement.
How to use
MD-KNEE can be used alone or in combination with other medical devices from the same line, in order to guarantee personalized treatment based on the individual clinical picture.
In cases where supportive treatment is required for the onset of acute pain, MD-KNEE can be combined with MD-NEURAL, MD-POLY and MD-MUSCLE (one or more of these).
Furthermore, in cases where tissue matrix support therapy is required or a slowing down of physiological aging is necessary, MD-KNEE can be combined with MD-MATRIX and MD-TISSUE.
Therapeutic protocol :
1 treatment per week for 10 consecutive weeks.
Method of administration: periarticular injection (the application area must be aseptic; insert the needle to a depth of 2-4 mm).
For this use of the medical device, the use of the following materials and accessories is recommended:
• Material to ensure skin asepsis: disposable glove, iodine-based solution, alcohol solution, sterile gauze, ethyl chloride-based skin spray.
• Needles: sterile 27 G.
• Syringes: 5 or 10 cc, depending on the quantity of solution to be injected.
Method of administration: intra-articular injection.
For this use of the medical device, the use of the following materials and accessories is recommended:
• Material to ensure skin asepsis: disposable glove, iodine-based solution, alcohol solution, sterile gauze, ethyl chloride-based skin spray. The application of local anesthetic on the treated skin is recommended.
• Needles: sterile 22 G.
• Syringes: 2 cc, depending on the quantity of solution to be injected.
Intra-articular injection treatment (inner side) :
The patient lies supine with the knee slightly flexed. Introduce a 22-gauge needle toward the plane of the posterior surface of the patella in the medial and lateral positions.
Components
Collagen of porcine origin.
Excipients: Arnica, NaCl, water for injection.
Warnings
Disposable.
No case of hypersensitivity has been reported.
Contains collagen of animal origin from porcine species. Patients with known hypersensitivity to the component or excipients should be previously subjected to an injection test in the arm and kept under observation for one hour.
Knee pain requires differential diagnosis with damage to the collateral or cruciate ligaments, prepatellar bursitis, painful hip pathologies, osteochondritis dissecans, predominantly inflammatory arthropathy, gout, septic arthritis.
Slight redness at the injection area may be due to the mechanical effect of the needle or a skin reaction.
The application may cause burning/pain symptoms at the injection sites, which generally resolve within 5-10 minutes after the end of treatment.
Skin cleaning/disinfection is required before and after application.
Any pyogenic bacteria may produce an abscess in the injection area.
Keep out of the reach and sight of children.
Do not use after expiration.
Use the product immediately after opening.
Do not use if seal is broken or tampered with.
After opening, the contents of the vial must be injected immediately.
Do not use if packaging is damaged.
Conservation
Store at a temperature between 2°C and 30°C, protect from sunlight and frost.
The expiry date refers to the product in its intact packaging, stored correctly.
Format
Pack of 5 sterile 2 ml vials