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46
Inflate the inner tube
1) Ensure that the valve is upright in order to achieve a good fit of inner tube and tyre in the valve area.
2) Screw on the valve nut firmly.
3) Inflate the inner tube until the tyre can still be depressed with your thumb.
INFORMATION If the indicator line has the same distance to the edge of the wheel rim all around and on
both side, the tyre is seated centrically. If not, let some air out and realign the tyre.
4) Inflate the inner tube to the maximum pressure indicated by the tyre manufacturer (see sidewall of tyre).
5) Screw the dust cap firmly onto the valve.
7 Disposal
7.1 Disposal information
In the case of disposal, return the wheelchair to the dealer.
All components of the product must be disposed of in accordance with the respective national environmental laws.
8 Legal information
8.1 Period of use
Based on market observations and the current state of technology, the manufacturer has calculated that the product
can be used for a period of
4 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.
It should be emphasised, however, that the product is reliable far beyond this defined period of time if it is cared for
and maintained properly.
If the end of the useful life is reached, the user or a responsible accompanying person should contact the qualified per
sonnel who supplied the wheelchair or the Otto Bock after-sales service (address, see rear inside cover or rear cover).
8.2 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 manu
facturer. Repairs must be carried out exclusively by authorised dealers or by the manufacturer.
8.3 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 criteria outlined in appendix IX of the guidelines. The declaration
of conformity was therefore created by Otto Bock with sole responsibility according to appendix VII of the guidelines.
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12/2010
Disposal
