medi Genumedi pro, Руководство пользователя

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Genumedi
®
pro
Intended purpose
Genumedi pro is a knee support brace without limitation of extension/
flexion.
Indications
All indications in which support of the physiological guidance of the knee
joint is necessary, such as:
• Light and medium instabilities of the knee joint
• Gonarthrosis
•
Mild collateral ligament instabilities
Contraindications
None known at present.
Risks / Side Effects
If the aids are too tight, this can cause local pressure sores or constriction
of blood vessels or nerves. Therefore you should consult the doctor
treating you before you use it if the following circumstances apply to you:
• Condition or injury of the skin in the area of application, particularly
with infectious indications (excessive heat, swelling or reddening)
•
Paraesthesia and circulatory disorders (e.g. as seen in diabetes, varicose
veins)
• Lymph drainage disorders – equally, swelling of soft tissue adjacent to
the area of application which is not related to a condition
When wearing snug-fitting aids, this can result in localised skin
inflammation or irritation that is due to mechanical irritation of the skin
(particularly in conjunction with sweating) or due to the composition of
the material.
Intended patient groups
Healthcare professionals should provide care to the adults and children,
applying the available information on the measurements/sizes and
necessary functions/indications and in line with the information provided
by the manufacturer, and acting under their own responsibility.
Note on wearing
Supports are most beneficial during physical activity. The support can in
principle be worn throughout the day. This must depend on how
comfortable the wearer is. Moreover, the knee may not be bent by more
than 70° when sitting. The support should be removed for long breaks
(e.g. long periods sitting, long drives or sleeping).
Putting on / Taking off
• Open both of the straps (Fig. 1).
•
Grasp the inside of the bandage with the thumb, at the upper end of the
lateral stabilisation rods. The grip-ons applied on the outer surface
serve as grip dots and make the support easier to put on (Fig. 2).
• Pull the bandage over the knee in such a way that the silicone ring goes
around the kneecap, so that it is positioned centrally and no pressure is
placed on the kneecap. The centre of the joint should now be level with
the upper edge of the kneecap (Fig. 3).
• Close both of the straps (Fig. 4).
•
Then check the bandage‘s position again.
• To remove the bandage, first open both straps. Then grasp the inside of
the bottom end of the bandage and pull it downwards and off (Fig. 5).
Care instructions
The silicone ring and the joints are not supposed to be removed when
washing the brace. Hook and loop fasteners should be closed for washing.
We recommend using a laundry bag. Fabric softener, fats, oils and
ointments can attack the material and the Clima Comfort Effect can be
impaired. Soap residues can cause skin irritation and material wear.
• 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, viscose
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 rapid 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
E016364-AAL_Genumedi_Pro.indd 5 04.11.21 12:38