Invacare Pronto M41 Series User Manual page 19

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.
1553378-G
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 provider
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.
Safety
19