Medi SAS multi Gebrauchsanweisung Seite 6

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shoulder and underarm straps
(Fig. 7).
6. Finally close the snap fastener. (Fig. 8).
The shoulder strap can be put on more
easily if you have a home help. Have
the person remove the shoulder strap
completely (open snap fasteners). They
can now help you into the shoulder strap
as if you were putting on a jacket.
(Fig. 7). Then proceed in the manner
described above. The shoulder strap is
then simply clicked into the cushion. If
you have the feeling during the night
that the arm or shoulder is not securely
positioned, you can put a pillow under
the brace or you can tighten the strap
around the waist.
In principle, this product must be used
under medical supervision. When it
is applied for the first time, this must
be under the instructions of trained
and specialised personnel, such as an
orthopaedic technician. If the support is
individually fitted by a qualified person,
this will ensure that it is effective and
comfortable.
If it is to be used with other products,
this must be discussed with the
prescribing doctor.
Care instructions
The product should not be worn in
water. Soap residues, lotions and
ointments can cause skin irritation and
material wear.
• Pillow case, bag and straps can be
washed by hand, preferably using
medi clean washing agent, or in the
washing machine with the delicate
cycle at 30°C using mild detergent
without fabric softener.
• 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
PU foam, polyamide
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 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 2, No. 65 of the Regulation (EU)
2017/745 (MDR). The traceability of this
product is assured via a UDI code .