Orthovisc - osteoarthritis treatment 3 syringes 2 ml

Product Description

CE medical devices, class III.

Indications

Orthovisc, sterile, pyrogen-free solution of sodium hyaluronate (15 mg/ml) dissolved in physiological saline.
They are indicated as viscoelastic supplements or substitutes for synovial fluid in human joints; they are suitable for the treatment of symptoms of human synovial joint dysfunction such as osteoarthritis.
The actions of both products are lubrication and mechanical support.

Directions for use and Dosage

Store at a temperature between 2° and 25°C.
Allow them to reach room temperature approximately 20-45 minutes before use.
Not for intravenous injection.
The required amount is slowly infused into the selected joint space through an ISO/ANSI compliant, non-rigid, fulcrum hypodermic needle of appropriate diameter.
The diameters used for knee injections are 18-21 gauge.
The final selection for any procedure must be determined by the physician.
The volume varies depending on the size of the joint space, but should not exceed 2 ml for the knee and other large joints or 1 ml for small joints.
It is up to the physician to determine the appropriate volume to ensure that the joint is not overfilled.
The recommended treatment regimen is 3 injections at one-week intervals for each treatment cycle, with a maximum treatment cycle for an individual joint in a 6-month period.
Remove any effusion from the joint prior to injecting the product.
Do not overfill the joint space.

Warnings

Normal precautions for injections of substances into joints are recommended. Only medical personnel competent in accepted injection techniques for the administration of agents into joint spaces should inject sodium hyaluronate for this application.
Do not use an excessive amount of sodium hyaluronate and keep the patient under close observation.
Do not overfill the space.
If pain increases during the injection, stop the injection and withdraw the needle.
In case of abnormal consequences from the administration of the products, patients should contact their doctor immediately.
Do not use if the inner package (pouch) is opened or damaged.
For intra-articular injection.
Not for intravenous injection.
The sale and use of this medical device are restricted to a physician or under the supervision of a physician.
Single use product.
Do not resterilize.

Contraindications

The following pre-existing conditions may constitute relative or absolute contraindications for the use of the products:

• known sensitivity to any of the ingredients contained in the two products;
• pre-existing infections of the skin region at the intended injection site;
• known joint infections;
• known systemic bleeding abnormalities.

The products may contain traces of gram-positive bacterial proteins and are contraindicated in patients with a history of similar allergies.

Format

Pack of 1 and 3 2 ml syringes.