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  • DEUTSCH, seite 10
Reporting obligation
In accordance with legal provisions
within the EU, patients and users are
obliged to report any serious incident
that occurs when using a medical
device to both the manufacturer and
the competent national authorities (in
Germany BfArM, Bundesinstitut für
Arzneimittel und Medizinprodukte, the
Federal Institute for Drugs and Medical
Devices) immediately.
Indications
Splay foot and painful consequences of
this in the mid-foot
Material Composition
45 % Nylon
30 % Rubber
20 % Elastane
3 % Polypropylene
2 % Polyester
This product contains Latex,
which can cause allergic
reactions.
english
Side effects
There are currently no known side
effects for any part of the body if the
product is used correctly. However, if the
product is too tight it can cause local
pressure points or constrict blood
vessels and nerves.

Contraindications

Consult your doctor before using this
product in the following cases:
– Skin diseases or injuries in the area
where the product is used, particularly
if you experience any signs of
inflammation such as redness, an
increase in temperature or swelling
– Feeling of numbness and circulatory
problems in the area where the
product is used
– Problems with lymphatic drainage
and unexplained swelling
Disposal
Please dispose of the product
according to local regulations after
the end of use.
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