Legal information
The manufacturer is not responsible for damages caused
by components and spare parts not approved by the manu
facturer. Repairs must be carried out exclusively by author
ised dealers or by the manufacturer.
9.3 CE Conformity
This device meets the requirements of the 93 / 42 / EEC
guidelines for medical devices. This device has been classi
fied as a class I device according to the classification cri
teria outlined in appendix IX of the guidelines. The declara
tion of conformity was therefore created by Otto Bock with
sole responsibility according to appendix VII of the
guidelines.
9.4 Warranty terms
Further information on the warranty terms can be provided
by the qualified personnel supplying the wheelchair or by
the Otto Bock after-sales service (addresses, see rear
inside cover or rear cover).
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B500 classic/advanced