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Medi Epico active Gebrauchsanweisung Seite 5

Ellenbogenorthese zur führung und stabilisierung mit extensions- und / oder flexionsbegrenzung

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  • DEUTSCH, seite 1
Putting on the support
• Open and loosen all straps. Pull the
support on. The arm that you are using
it on should be bent slightly. Your palm
should be facing upwards (fig. 4).
• The guide line should be level with the
bend in your elbow (fig. 5). Check that
the support is positioned correctly by
bending and straightening your elbow.
• Fasten all of the ends of the straps in
the correct order (see numbering) and
check that the support is positioned
correctly again (fig. 6).
• The strap may be cut to the length
required by the individual. To this end,
open the hook and loop fasteners at
the ends of the straps and shorten the
straps accordingly (fig. 7).
• If necessary, the enclosed cushion can
be attached to the external side,
between the joint pocket and arm
(fig. 8).
Care instructions
Please close the hook and loop fasteners
before washing and remove the splint
(fig. 1). 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, polyamide, elastane, PU
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
English
.

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