Medi Epico ROMs Kidz Gebrauchsanweisung Seite 6

English
Fitting instructions
Open all of the hook-and-loop straps
and put the brace on the child/patient so
that the brace articulation is positioned
exactly over the lateral epicondyle (Fig.
5).
The length of the hand support can be
set using both of the screws on the lower
arm splint.
Fasten both of the underarm straps first,
and then the upper arm straps (Fig. 6+7).
Bring the end of the neck strap through
the eye on the upper arm sleeve and
close the hook-and-loop fastening. Bring
the other end around the shoulder, feed
it through the eye on the hand support,
and stick the end down (Fig. 8).
The neck pad can be moved to suit the
individual but should be positioned
centrally over the shoulder. The pads can
be trimmed to size using scissors, if
necessary.
Important notes
Adjust the extension and flexion limits
on the instructions of your doctor only.
Particularly during the first few days
after traumatic events, the belts should
be slackened often so as to avoid severe
swelling.
Care instructions
Hook and loop fasteners should be
closed for washing. Soap residues,
lotions and ointments can cause skin
irritation and material wear. The cushion
for the hand support can be removed for
washing. To remove the cushion, loosen
the screw of the shoulder strap with the
attached Allen key.
• Wash the paddings and straps by
hand, preferably using medi clean
washing agent.
• Do not bleach.
• Leave to dry naturally.
• Do not iron.
• Do not dry clean.
With normal use, the hinge mechanism
should not require any maintenance, but
it can be lubricated with PTFE spray.
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Storage instructions
Keep the product 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.
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 .