Bort CoxaPro Instruction Manual page 17

EN
After this, you can remove the guide flap 6 from the pelvis buckle. Then, remove the pelvis buckle from
the knitted fabric Velcro connection. The guide flap 6 is then attached directly to the velour which is on
the brace's knitted fabric.
In order to use the brace without the pelvis buckle and joint, thread the narrow straps 3 through the
guide loops 4 on the guide flap 6 towards the "bulging sail" on the front fastener. This ensures that the
brace also sits correctly and comfortably when downgraded.
The illustration shows the components already removed.
Removal
To remove the brace, please loosen the circular restraint around the thigh and open the frontal fasteners
around the hip. Following this, you can remove the brace.
Material composition
Cotton (CO), Polyamide (PA), elastodiene/latex (ED), elastane (EL), viscose (CV)
The sewn in textile label provides the precise material composition.
The product contains latex and can trigger allergic reactions.
Cleaning information
Delicate wash 30 °C Do not bleach (only wash with colour or mild detergents) Do not dry in a
tumble dryer Do not iron Do not clean chemically
Before washing, remove the pelvis buckle with the joint splint and close the Velcro fasteners in order to
avoid damaging other clothes items. Do not use fabric conditioner. Stretch back into shape and dry in the
fresh air.
Guarantee
The legal regulations of the country in which you acquired the product apply to the purchased product.
Please contact your specialist retailer if you suspect a warranty claim. Please clean the product before
submitting a warranty claim. If the enclosed instructions for use have not been properly observed, the
warranty may be impaired or cancelled. The warranty does not cover use of the product inappropriate for
the indication, non-observance of application risks, instructions and unauthorised modifications to the
product.
Useful life/Lifetime of the product
The lifetime of the medical device is determined by its natural wear and tear if treated appropriately and as
recommended.
Duty of notification
If a serious worsening of the state of health occurs when using the medical device, you are obliged to
notify the specialist dealer or us as the manufacturer and the Medicines & Healthcare products Regulatory
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