Otto Bock 50K13N Genu Arexa, Инструкция по эксплуатации, Страница: 14 / 108

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5.4 Cleaning
INFORMATION
► Ensure proper alignment when inserting the tibia pad. The wide side of the pad must face
up.
1) Remove the straps and pads from the brace.
2) Fasten all hook-and-loop closures.
3) Hand-wash the straps and pads in warm water at
30 °C (86 °F) using neutral detergent. Rinse
thoroughly.
4) Allow to air dry. Do not expose to direct heat sources (e.g. sunlight, stove or radiator).
5) If the brace comes into contact with salt water or dirt, rinse with clear water and allow to air
dry.
5.5 Information on re-use (applies for Germany only)
The product is approved for re-use exclusively in Germany. Products that are being re-used are
subject to increased strain. Re-use is only permitted up to a maximum total period of use of
2 years
.
Reconditioning
Hygienic reconditioning of the product (according to the Robert-Koch Institute guidelines) is
required prior to re-use.
All components subject to pronounced wear or that come into direct contact with skin are not suit­
able for re-use. These components are contained in the 29K110N replacement kit.
All components suitable for re-use must be checked for proper functionality and damage prior to
re-use.
5.5.1 Replacing the Straps and Pads
Straps:
1) The upper and lower straps can be released from the frame using the quick-release locks.
2) For the straps closest to the knee, remove the strap attachment caps on the outside of the
frame.
3) Release the plastic pin from the frame, insert the new strap and secure with the cap.
Strap and Frame Pads
The strap and frame pads are attached with hook-and-loop closures and are easy to replace.
6 Disposal
Dispose of the product in accordance with national regulations.
7 Legal Information
All legal conditions are subject to the respective national law of the country of use and may vary
accordingly.
7.1 Liability
The manufacturer shall be liable in the event that the product is used in accordance with the
descriptions and instructions in this document. The manufacturer will not assume liability for dam­
age caused by disregarding the information in this document, particularly due to improper use or
unauthorized modification of the product.
7.2 CE Conformity
This product meets the requirements of the European Directive 93/42/EEC for medical devices.
This product has been classified as a class I device according to the classification criteria out­