6
7
– no re-use – this medical aid is intended for treating one patient
– whilst wearing the support, please neither use any creams nor
ointments on or around it as they can destroy the material
– in order to avoid damages to the knitted support fabric, only attach
the Stabilo strap after successfully determining the size and trial
fitting. Goods damaged by the Velcro fastening cannot be returned.
Fitting instructions
Place the support on the metacarpophalangeal joint affected and guide
the thumb through the intended thumb opening at the same time. The
plastic splint runs along the surface of the palm. The Stabilo fleece strap
included can be fitted individually dosed. For this, attach the Stabilo
fleece strap to the velour on the support intended for this purpose using
the narrow Velcro strip. The Stabilo fleece strap can then be twisted
around the wrist circumferentially.
If required, the plastic splint material can be individually adapted by an
orthopaedic technician at a temperature of approx. 180°C. Let the
reshaped splint cool down and then re-insert it into the support splint
bag.
Removal
To remove the support, please loosen the Stabilo fleece strap. Grasp the
splint in the palm area and pull the support off over the fingers. Close
the Velcro fastener in order to avoid early wear to the Velcro surface.
Material composition
Polyamide (PA), elastodiene/latex (ED), elastane (EL)
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 clothes dryer
Do not iron
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 the
manufacturer and the Medicines & Healthcare products Regulatory
Agency (MHRA).
You can find the manufacturer’s contact data in these instructions
for use. You can find the contact information for the appointed
authority for your country under the following link: www.bort.com/
md-eu-contact.
Disposal
Upon the termination of use, the product must be disposed of in
accordance with the corresponding local requirements.
Declaration of conformity
The manufacturer confirms that this device conforms with the
requirements of REGULATION (EU) 2017/745 OF THE EUROPEAN
PARLIAMENT AND OF THE COUNCIL.
Status: 02.2020
Medical device |
Single patient – multiple use
