medi protect.St, Инструкция по эксплуатации

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wedges or 0° wedges. The wedges define
the exact excursion of the orthosis. In
difficult soft-tissue conditions, e.g.
where the soft-tissues are under
compression, it may be necessary to
insert the larger wedge to limit the joint
movement to the desired excursion. In
addition, make sure that the orthosis
joints are correctly positioned: the
middles of the joints should be level with
the upper border of the patella. The joint
must lie behind the midline of the leg.
Fitting instructions
•
Open all straps and the two hook and
loop fasteners.
• Now put your leg into a 45-degree
angle flexion position. Wrap the
orthosis tightly around your leg from
the back and close it with the two hook
and loop strips (Image 1),
• Make sure that the kneecap is in the
middle of the patella recess.
• The centres of the brace joints should
be at the top edge of the kneecap and
just behind the lateral centre line of
the leg (image 2).
• Now close the bottom strap and then
the top strap (image 3).
• If possible, walk a few steps and check
if the brace is properly fitted (image 4).
Correct the fit of the brace at the leg, if
required.
Care instructions
Please close the hook and loop fasteners
before washing and remove the
ortheses. 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 brace in a dry place and do not
expose to direct sunlight.
Material composition
Polyamide, elastane, PU, aluminum,
polyester
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
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
E011578_AAL_protect_ST_III.indd 5 15.03.21 13:39