KNEE BRACE WITH ORTHOPEDIC STAYS
Closed knee brace AM-OSK-Z/S-P is made of innovative fabric ActivePren™.
ActivePren™ is an active 3-layered fabric made of elastic jersey layer and perforated neoprene foam. This lamination is very soft and high elastic. Foam’s perforation improves the air circulation and maintains great skin’s condition. The skin can breathe freely and its required temperature is maintained because of AirSupply System. This material is not knitte, what prevents skin against the skin abrasions in the compression zones. Our braces, made of ActivePren are the most durable and provide the best stabilization in the market. WATERPROOF MATERIAL.
The brace is equipped with independent sets of reinforcement straps made of VELCRO tape, elastic orthopaedic stays and anatomically kneecap support with antimycotic properties which stabilizes patella precisely.
Purpose of use
AM-OSK-Z/S-P brace should be applied in cases of:
- knee dislocation,
- knee twist and sprain,
- side instability of the knee joint,
- knee ligaments LCL, MCL and ACL injuries,
- other surgeries (orthopedic),
- as an prevention against kneecap instability (patellar subluxation)
|Size||Knee circumference||How to measure|
|S||29 cm (11,4″)|
|L||30 cm (11,8″)|
Our orthopedic spiral boning is a thin wire, coiled into a spring and flattened. We use boning of various widths and wire thicknesses, which determines the strength of their stabilization. Each spiral boning has two specially profiled fittings to prevent damage of the orthosis. They are galvanically protected against corrosion by the galvanizing process, so they are resistant to water, moisture and sweat. Products equipped with bonings can be washed without removing them from the orthosis. They work in every direction, perfectly adjusting to the user's body and have a shape memory function, thanks to which they always return to their original profile. This function causes the spiral boning in the orthosis to stabilize the swollen limb immediately after the injury and after the swelling has come off.
Class I medical device in accordance with Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017. on medical devices.