medi ROM Walker Mode D'emploi page 6

English
Place your foot in the padding so that
the heel stands firmly in the pre-
formed heel bed and close the padding
(B). Patients with very slim calves can
trim the pad to the right length using
scissors if there is a large overlap of the
padding.
• Place your foot in the rigid shell of the
Walker. The two guide supports should
lie exactly along the middle of the
inside and outside of the calf.
Then close both the hook and loop
fasteners of the foot section and the
back heel strap (C).
• Finally fasten the three leg straps from
the bottom up (D). Make sure that the
straps lie flat against the pad and are
tightly closed at the front. However, be
careful not to impair the blood
circulation.
For additional stabilisation of the lower
leg the enclosed plastic shells can be
fixed to the pad. The broader one is
intended for the calf area. The padding
can be used for additional cushioning
(e.g. across the instep, at the heel strap,
between the ankle bone and joint).
Important notes
Only change the extension and flexion
limits on instruction from your doctor or
orthotist to do so.
Care instructions
Hook and loop fasteners should be
closed for washing. Soap residues,
lotions and ointments can cause skin
irritation and material wear.
· Wash the paddings by hand, preferably
using medi clean washing agent.
· Do not bleach.
· Leave to dry naturally.
· Do not iron.
· Do not dry clean.
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Storage instructions
Keep the brace in a dry place and do not
expose to direct sunlight.
Material Composition
Aluminum, PU-foam, cotton
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.
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 .