Otto Bock B500 plus, Instructions For Use Manual, Page: 20 / 28

20 | Ottobock B500 plus
Disposal
► Note that the batteries may not be disposed of as
household waste.
All product components must be disposed of properly in
accordance with national regulations.
9.2 Information on Re-Use
CAUTION
Use of used seat upholstery
Functional and hygiene risks for the skin
► Replace the seat upholstery if the wheelchair is to be
re-used.
The product is suitable for re-use.
Similar to second-hand machines or cars, products that are
being re-used are subject to increased strain. Features and
functions must not change in a way that could endanger
patients or other persons within the product’s lifespan.
Based on market observations and the current state of tech­
nology, the manufacturer has calculated that the product
can be used for a period of
5 years
, provided that it is used
properly and that the service and maintenance instructions
are observed. Storage times at the dealer or with paying
parties are not included in this period. However, we would
like to emphasise that the product is reliable far beyond this
defined period of time, provided that it is cared for and
maintained properly.
The product must first be thoroughly cleaned and disinfec­
ted before it can be re-used. Then the product must be
examined by an qualified specialist to check the condition
and to look for wear and possible damage. All worn and
damaged parts as well as components which do not fit or
are unsuitable for the new user must be replaced.
Detailed information on replacing components as well as
information on the required tools and the prescribed service
intervals can be found in the service manual.
10 Legal Information
All legal conditions are subject to the respective national
laws of the country of use and may vary accordingly.
10.1 Liability
The manufacturer will only assume liability if the product is
used in accordance with the descriptions and instructions
provided in this document. The manufacturer will not
assume liability for damage caused by disregard of this doc­
ument, particularly due to improper use or unauthorised
modification of the product.
10.2 CE Conformity
This product meets the requirements of the European Dir­
ective 93
/ 42 / EEC for medical devices. This product has
been classified as a class I device according to the classific­
ation criteria outlined in Annex IX of the directive. The
declaration of conformity was therefore created by the man­