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Medi Spinomed Gebrauchsanweisung Seite 8

Rückenorthese bei osteoporose
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osteoporosis. The Spinomed stimulates
the body's own muscle resources. The
back splint will have been individually
adjusted by your orthopaedic
technician. Together with the straps, the
brace supports your muscles in holding
your shoulders back and straightening
your upper body. You will still be able to
freely move your shoulders and arms as
well as breathe unhindered. If the brace
has been optimally adjusted, it can
reduce pain and increase day-to-day
mobility.
Application
While you are getting used to the brace
and to progressively re-establish muscle
activity, wearing of the brace should be
gradually increased. This means that you
should wear the Spinomed a little longer
each day, gently training the muscles.
Depending on physical condi tion, an
uninterrupted wearing time of
minutes will be sufficient at the
beginning, which is then gradually
increased.
Care instructions
The aluminum splint must be removed
before washing. Hook and loop fasteners
should be closed for washing. 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 product in a dry place and do
not expose to direct sunlight.
Material composition
Aluminum, polyester, elastane,
elastomer
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
, No.
of the Regulation (EU)
(MDR). The traceability of this product is
assured via a UDI code
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