MD-KNEE

Description
Useful medical device for improving knee joint mobility, whose main therapeutic treatment consists of the following functions:
1. Barrier effect.
2. Lubricating activity.
3. Mechanical support in case of continuous drug therapy.
The use of MD-KNEE is recommended by qualified medical personnel in private or public healthcare facilities for:
- improves knee mobility;
- promotes muscle relaxation;
- relieves knee pain and pain projected during movement.

How to use
MD-KNEE can be used alone or in combination with other medical devices from the same line, to ensure personalized treatment according to 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).
In addition, in cases where tissue matrix support therapy is required or where a slowdown in physiological aging is required, 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; the needle is inserted to a depth of 2-4 mm).
For this use of the medical device, the following materials and accessories are recommended:
• Material to ensure skin asepsis: disposable glove, iodine-based solution, alcohol-based solution, sterile gauze, ethyl chloride-based skin spray.
• Needles: sterile 27 G.
• Syringes: 5 or 10 cc, depending on the amount of solution to be injected.

Method of administration: intraarticular injection.
For this use of the medical device, the following materials and accessories are recommended:
• Materials to ensure aseptic conditions of the skin: disposable gloves, iodine solution, alcohol solution, sterile gauze, ethyl chloride skin spray. It is recommended to apply a local anesthetic to the treated skin.
• Needles: sterile 22 G.
• Syringes: 2 cc, depending on the amount of solution to be injected.

Intra-articular injection treatment (inside) :
The patient is in the supine position with the knee slightly flexed. A 22-gauge needle is inserted into the medial and lateral planes of the posterior surface of the patella.

components
Collagen of porcine origin.
Excipients: Arnica, NaCl, water for injections.

warnings
Disposable.
No cases of hypersensitivity have been reported.
Contains porcine collagen. Patients with known hypersensitivity to the component or excipients should undergo a preliminary injection test in the arm and be observed for one hour.
Knee pain requires differential diagnosis with collateral or cruciate ligament damage, prepatellar bursitis, painful hip conditions, osteochondritis dissecans, predominantly inflammatory arthropathy, gout, and septic arthritis.
Slight redness at the injection site may be caused by the mechanical effect of the needle or a skin reaction.
Application may cause symptoms of burning/pain at the injection sites, which generally disappear within 5-10 minutes after the end of treatment.
Skin cleansing/disinfection is necessary before and after application.
Any pyogenic bacteria could cause an abscess at the injection site.
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 should be injected immediately.
Do not use if the packaging is damaged.

Conservation
Store between 2°C and 30°C, away from sunlight and frost.
The expiration date refers to the product in its intact packaging, stored correctly.

Format
Pack of 5 sterile 2 ml vials