Optional - Only 50R232 Smartspine Lso High: Remove Components; Legal Information - Ottobock 50R232 Smartspine LSO high Instrucciones De Uso

5) Optional – shortening the pull cable: Pull the winding card out of the pocket (see fig. 5),
wrap the pull cable around the winding card (see fig. 6), and put the winding card back into
the pocket.
4.4 Optional – only 50R232 Smartspine LSO high: Remove components
The side parts, the abdomen part, and the back part can be removed. The removal of the compo­
nents is directed by the physician.
Side parts
1) Open the hook-and-loop closures between the side parts and back part.
2) Remove the side parts. In order to do so, pull the side parts over the abdomen part (see
fig. 7).
Abdomen part
1) Open the hook-and-loop closures on the abdomen part (see fig. 8).
2) Remove the abdomen part.
Back part
1) Open the hook-and-loop closure on the back part.
2) Remove the elastic bands from the back plate (see fig. 1).
3) Close the hook-and-loop closures on the back part.
4) Remove back part. In addition, pull the abdominal strap out of the back part.
4.5 Cleaning
NOTICE
Use of improper cleaning agents
Damage to the product due to use of improper cleaning agents
► Only clean the product with the approved cleaning agents.
Clean the brace regularly:
1) Remove all boards/plates.
2) Fasten all hook-and-loop closures.
3) Hand wash the brace in warm water at 30 °C with standard mild detergent.
4) Rinse well.
5) Allow to air dry. Do not expose to direct heat sources (e.g. sunlight, stove or radiator).
5 Disposal
Dispose of the product in accordance with national regulations.

6 Legal Information

All legal conditions are subject to the respective national law of the country of use and may vary
accordingly.
6.1 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.
6.2 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
lined in Annex IX of the directive. The manufacturer therefore drew up the declaration of conformi­
ty on its own responsibility in accordance with Annex VII of the directive.
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