bort medical 104 730, Инструкция по эксплуатации

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become necessary to reduce the stabilising effect of the BORT StabiloPlus Back support. This decision is
taken by the treating physician. For this, remove the more rigid version of the splints from the externally
attached splint bag by folding the restraints back and removing the splints through the slit in the splint
bag. The shorter, more flexible splints can then be inserted. The bridging segment can also be removed
from its cloth bag and replaced with two splints. For this, remove the cloth bag including the bridging
segment from the BORT StabiloPlus Back support, take the bridging segment out of the cloth bag from
the rear slit and insert two of the longer, more flexible splints into the holders in the cloth bag designated
for this purpose. Finally, attach the cloth bag back to the BORT StabiloPlus; here the wide side facing the
direction of the head.
Removal
To remove the brace, open the tension straps and the front fastening and take the brace off.
Material composition
Elastodiene/latex (LA), polyamide (PA), 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 Do not clean chemically Do not bleach
Do not dry in a tumble dryer Do not iron
Do not use fabric conditioner. Stretch back into shape and dry in the fresh air. Close the Velcro fastening to
avoid damage to other laundry items.
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
Agency (MHRA).