Ottobock | 19
B500 Family
►
Observe the information printed on the batteries by the
manufacturer.
►
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
10.1 Liability
The manufacturer’s warranty applies only if the device has
been used under the conditions and for the purpose
described. The manufacturer recommends that the device
be used and maintained according to the instructions for
use.
The manufacturer is not responsible for damages caused by
components and spare parts not approved by the manufac
turer. Repairs must be carried out exclusively by authorised
dealers or by the manufacturer.
10.2 CE Conformity
This device meets the requirements of the 93 / 42 / EEC
guidelines for medical devices. This device has been classi
Legal Information
