Invacare Wheelchair Pronto M61, Руководство пользователя

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Safety
CAUTION!
Risk of injuries and damage to mobility device due
to unapproved components and accessory parts
Seating systems, additions and accessory parts which
have not been approved by Invacare for use with
this mobility device can affect the tipping stability and
increase tipping hazards.
–
Only ever use seating systems, additions and accessory
parts which have been approved by Invacare for this
mobility device.
Seating systems which are not approved by Invacare
for use with this mobility device do not, under certain
circumstances, comply with the valid standards and could
increase the flammability and the risk of skin irritation.
–
Only use seating systems that have been approved by
Invacare for this mobility device.
Electrical and electronic components which have not
been approved by Invacare for use with this mobility
device can cause fire hazards and lead to electromagnetic
damage.
– Only ever use electrical and electronic components
which have been approved by Invacare for this
mobility device.
Batteries which have not been approved by Invacare for
use with this mobility device can cause chemical burns.
–
Only ever use batteries which have been approved by
Invacare for this mobility device.
CAUTION!
Risk of injuries, and damage to the mobility
device, if unapproved backrests are used
A retrofitted backrest which is not approved by Invacare
for use with this mobility device may overload the
backrest tube and thus increase the risk of injuries and
of damage to the mobility device.
–
Please contact your Invacare specialist dealer who will
perform risk analyses, calculations, stability checks etc.
to ensure that the backrest can be used safely.
CE marking of the mobility device
– The conformity assessment/CE marking was carried
out in accordance with Directive 93/42 EEC and only
applies to the complete product.
–
The CE marking is invalidated if components or
accessories are replaced or added that have not been
approved for this product by Invacare.
– In this case, the company that adds or replaces the
components or accessories is responsible for the
conformity assessment/CE marking or for registering
the mobility device as a special design and for the
relevant documentation.
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