Descrizione Clinica
Medical devices - medical devices Md-knee 5fl injectable 2ml Guna
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. Lubricant activity.
3. Mechanical support in case of ongoing drug therapy.
It is recommended to use MD-KNEE by qualified health personnel, at private or public health facilities for:
- improve knee mobility;
- promote muscle relaxation;
- relieve knee pain and projected during movement.
Mode of use
MD-KNEE can be used alone or associated with other medical devices belonging to the same line, in order to ensure a personalized treatment based on the individual clinical framework.
In cases where acute pain is required, MD-KNEE may be associated with MD-NEURAL, MD-POLY and MD-MUSCLE (one or more of these).
In addition, in cases where a tissue matrix support therapy is required or a slowdown of physiological aging is required, MD-KNEE may be associated with MD-MATRIX and MD-TISSUE.
Therapeutic protocol:
1 treatment per week for 10 consecutive weeks.
Periarticular injectable mode of administration (the application area must be aseptic; introduce the needle to a depth of 2-4 mm).
For this use of the medical device it is recommended to use the following materials and accessories:
• Material to ensure skin axle: disposable glove, iodine based solution, alcohol solution, sterile garzes, skin spray based on ethyl chloride.
• Needles: 27 G sterile.
• Syringes: from 5 to 10 cc, according to the amount of solution to inject.
Injectable intraarticular mode of administration.
For this use of the medical device it is recommended to use the following materials and accessories:
• Material to ensure skin axle: disposable glove, iodine based solution, alcohol solution, sterile garzes, skin spray based on ethyl chloride. We recommend the application of local anesthetic on the treated skin.
• Needles: 22 G sterile.
• Syringes: 2 cc, according to the amount of solution to inject.
Injective intraarticular treatment (internal side):
The patient lies supine with the slightly flexed knee. Introduce a 22 G needle to the back surface of the patella in a medial and lateral position.
Components
Collagen of suine origin.
Excipients: Arnica, NaCl, injectable water.
Warnings
Disposable.
No case of hypersensitivity has been reported.
Contains collagen of animal origin of suine species. Patients with proven hypersensitivity to the component or excipients should be previously subjected to injective testing in the arm and kept under observation for an hour.
Gonalgies require differential diagnosis with damage to collateral or crusader ligaments, pre-patellar borsites, algical pathologies at the hip, declining osteochondrite, arthritis with a predominantly inflammatory character, gout, septic arthritis.
A slight redness in the injection area can be due to the mechanical effect of the needle or a skin reaction.
The application may cause symptoms of burning/dollar in injection sites, which generally resolve within 5-10 minutes from the end of treatment.
Skin cleaning/disinfection is necessary before and after application.
Any pyogenic bacteria could produce abscess in the injection area.
Keep out of reach and sight of children.
Do not use after expiry.
Use the product immediately after opening.
Do not use in case of breakage or tampering of the seal.
After opening, the contents of the bottle must be injected immediately.
Do not use in case of packaging damage.
Conservation
Store at a temperature of 2°C and 30°C, protect against sunlight and frost.
The expiration date refers to the product in an integrated package, properly preserved.
Format
Pack of 5 2 ml sterile bottles
Medical device useful for improving the mobility of the knee joint, whose primary therapeutic treatment consists of the following functions:
1. Barrier effect.
2. Lubricant activity.
3. Mechanical support in case of ongoing drug therapy.
It is recommended to use MD-KNEE by qualified health personnel, at private or public health facilities for:
- improve knee mobility;
- promote muscle relaxation;
- relieve knee pain and projected during movement.
Mode of use
MD-KNEE can be used alone or associated with other medical devices belonging to the same line, in order to ensure a personalized treatment based on the individual clinical framework.
In cases where acute pain is required, MD-KNEE may be associated with MD-NEURAL, MD-POLY and MD-MUSCLE (one or more of these).
In addition, in cases where a tissue matrix support therapy is required or a slowdown of physiological aging is required, MD-KNEE may be associated with MD-MATRIX and MD-TISSUE.
Therapeutic protocol:
1 treatment per week for 10 consecutive weeks.
Periarticular injectable mode of administration (the application area must be aseptic; introduce the needle to a depth of 2-4 mm).
For this use of the medical device it is recommended to use the following materials and accessories:
• Material to ensure skin axle: disposable glove, iodine based solution, alcohol solution, sterile garzes, skin spray based on ethyl chloride.
• Needles: 27 G sterile.
• Syringes: from 5 to 10 cc, according to the amount of solution to inject.
Injectable intraarticular mode of administration.
For this use of the medical device it is recommended to use the following materials and accessories:
• Material to ensure skin axle: disposable glove, iodine based solution, alcohol solution, sterile garzes, skin spray based on ethyl chloride. We recommend the application of local anesthetic on the treated skin.
• Needles: 22 G sterile.
• Syringes: 2 cc, according to the amount of solution to inject.
Injective intraarticular treatment (internal side):
The patient lies supine with the slightly flexed knee. Introduce a 22 G needle to the back surface of the patella in a medial and lateral position.
Components
Collagen of suine origin.
Excipients: Arnica, NaCl, injectable water.
Warnings
Disposable.
No case of hypersensitivity has been reported.
Contains collagen of animal origin of suine species. Patients with proven hypersensitivity to the component or excipients should be previously subjected to injective testing in the arm and kept under observation for an hour.
Gonalgies require differential diagnosis with damage to collateral or crusader ligaments, pre-patellar borsites, algical pathologies at the hip, declining osteochondrite, arthritis with a predominantly inflammatory character, gout, septic arthritis.
A slight redness in the injection area can be due to the mechanical effect of the needle or a skin reaction.
The application may cause symptoms of burning/dollar in injection sites, which generally resolve within 5-10 minutes from the end of treatment.
Skin cleaning/disinfection is necessary before and after application.
Any pyogenic bacteria could produce abscess in the injection area.
Keep out of reach and sight of children.
Do not use after expiry.
Use the product immediately after opening.
Do not use in case of breakage or tampering of the seal.
After opening, the contents of the bottle must be injected immediately.
Do not use in case of packaging damage.
Conservation
Store at a temperature of 2°C and 30°C, protect against sunlight and frost.
The expiration date refers to the product in an integrated package, properly preserved.
Format
Pack of 5 2 ml sterile bottles
