Fitting Instructions; Care Instructions; Material Composition - medi Stabimed Instrucciones De Uso

English
addition, make sure that the orthosis
joints are correctly positioned: the
middles of the joints should be level with
the upper border of the patella. The joint
must lie behind the midline of the leg.

Fitting instructions

• Open all straps and the two hook and
loop fasteners. Pull the two straps
back a little so they don't hamper you
when you put the brace on.
• Now put your leg into a
angle flexion position. Wrap the brace
tightly around your leg from the back
and close it with the two hook and
loop strips (image ),
• Make sure that the kneecap is in the
middle of the patella recess.
• The centres of the brace joints should
be at the top edge of the kneecap and
just behind the lateral centre line of
the leg (image ).
• Now close the bottom strap and then
the top strap (image ).
• If possible, walk a few steps and check
if the brace is properly fitted (image ).
Correct the fit of the brace at the leg, if
required.

Care instructions

Please close the hook and loop fasteners
before washing and remove the ortheses
(image , , ). Soap residues, lotions and
ointments can cause skin irritation and
material wear.
• Wash the product by hand, preferably
using medi clean washing agent.
• Do not bleach.
• Leave to dry naturally.
• Do not iron.
• Do not dry clean.
Storage instructions
Keep the brace in a dry place and do not
expose to direct sunlight.

Material composition

Avional, polyamide, elasthane, PU
Liability
The manufacturer's liability will become
void if the product is not used as
intended. Please also refer to the
corresponding safety information and
instructions in this manual.
-degree
Disposal
The product can be disposed of
in the domestic waste.
Your medi team
wishes you a quick return to full fitness.
In the event of any complaints regarding
the product such as damage to the fabric
or a fault in the fit, please report to your
specialist medical retailer directly. Only
serious incidents which could lead to a
significant deterioration in health or to
death are to be reported to the
manufacturer or the relevant authorities
in the EU member state. The criteria for
serious incidents are defined in Section
, No.
(MDR). The traceability of this product is
assured via a UDI code
of the Regulation (EU)
.
/