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Beschikbare talen
Beschikbare talen
side (Fig. 3).
• Wrap the support around your body
and check once again on the label that
you have the orthotic the right way
around (Fig. 4) .
• Now, slide your right hand into the
outer hand strap on the right-hand
fastener side (Fig. 5).
• Pull both fastener sides together in the
middle, so that they can be fixed over
each other as far at the same distance.
When fastening, ensure that the back
brace is in the middle (Fig. 6 + 7).
The orthotic is on properly when the
lower fastener edge is just above the
pubic bone (see Fig. 8).
• Now unfasten the strap ends of both
lower pull straps and pull these
forward at the same time. You can
adjust the tightness to suit your own
requirements and manage your pain
levels (Fig. 8 + 9).
• Do the same for the upper pull straps
(Fig. 10 + 11).
• Information for technicians: The strap
length may be adjusted by cutting it at
the edge of the Y fastener (Fig. 12).
Care instructions
Hook and loop fasteners should be
closed for washing. We recommend
using a laundry bag. Fabric softeners,
fats, oils, lotions, ointments and soap
residues can affect the material, hinder
the Clima Comfort effect and cause skin
irritations.
• You can wash the product by hand,
preferably using a medi clean
detergent, or in delicate cycle at 30°C
using a mild detergent without fabric
conditioners.
• 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
Polyamide, Polyester, Elastane
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).
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