Storage Instructions - Medi Ankle sport brace Gebrauchsanweisung

English
under the middle portion of the sole of
the foot (Fig. 4)
• Now grip the loop of the strap with a
finger and pull it up the side of your
leg. Fasten the strap slightly above the
ankle joint. When doing this, ensure
that your foot is in a neutral position
(at 90° to your leg) (Fig. 5)
• Now take the inside strap and pull it
over the arch of your foot (instep) to
the outside of your foot and then feed
it under the middle portion of the sole
of the foot (Fig. 6)
• Now grip the loop of the strap with a
finger and pull it up the side of your
leg. Fasten the strap slightly above the
ankle joint (Fig. 7)
• Now do up the belt that goes around
the circumference of the leg (Fig. 8)
• Check that the brace fits snugly and
that you feel stable in it (Fig. 9)
• The brace can be altered or adjusted
according to your requirements at any
time. To achieve this, you can change
the position of or remove the straps
around the heel (Fig.10) and also move
or remove the stabilising shells (Fig. 11)
Care instructions
Please remove the stabilising shells at
the sides and fasten the the hook and
loop fasteners before you wash the
brace. Soap residues, lotions and
ointments can cause skin irritation and
material wear.
• Wash the product by hand, preferably
using a medi clean detergent, or in
delicate cycle at 30°C using a mild
detergent without fabric conditioners.
• Do not bleach.
• Leave to dry naturally.
• Do not iron.
• Do not dry clean.
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Storage instructions

Keep the product in a dry place and do
not expose to direct sunlight.
Material composition
Polyamide, polyester, polyethylene
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.
Disposal
The product can be disposed
of in the domestic waste.
Your medi team
Wishes you a speedy recovery!
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
2, No. 65 of the Regulation (EU) 2017/745
(MDR). The traceability of this product is
assured via a UDI code .