Genu Ligaflex® ROM
Genu Ligaflex® ROM

Genu Ligaflex® ROM

Genu Ligaflex® ROM

Properties/Mode of action

  • Stabilization of knee joint ligaments provided by the rigid hinged side uprights.
  • - Extension can be adjusted to 0°, 5°, 10°, 15°, 20°, 30° and 40°.
  • - Flexion can be adjusted to 0°, 30°, 45°, 60°, 75° and 90°.
  • The brace is maintained on the leg thanks to:
  • - the Suspension Strap (A);
  • - the silicone-coated threads at the top of the knee brace.
  • Model totally open, making it easy to fit.



Verify the product’s integrity before every use.

Do not use the device if it is damaged.

Choose the appropriate size to fit the patient, referring to the size chart; not applicable to the medical devices made to measure patient, the measures are individually taken.

It is recommended that a healthcare professional supervises the first application.

Strictly comply with your healthcare professional’s prescription and recommendations for use.

This product is intended for the treatment of a given condition. Its duration of use is limited to this treatment only

For hygiene and performance reasons, do not re-use the product for another patient.

It is recommended to adequately tighten the device to achieve support/immobilisation without restricting blood circulation.

In the event of discomfort, significant hindrance, pain, variation in limb volume, abnormal sensations or change in colour of the extremities, remove the device and consult a healthcare professional.

In the event of any modification in the product's performance, remove it and consult a healthcare professional

Do not wear the product in a medical imaging device.

Do not use the device in case of application of certain products on the skin (creams, ointments, oils, gels, patches...).

Undesirable side-effect:

This device can cause skin reactions (redness, itching, burns, blisters...) or wounds of various degrees of severity.

Any serious incident occurring related to the device should be reported to the manufacturers and to the competent authority of the Member State in which the user and/or patient is resident.


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