Invacare Modulite Bora XTR Series, Руководство по обслуживанию

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Invacare® Modulite
1 General
1.1 About this manual
• This document is a supplement to the power wheelchair’s
documentation.
•
The product itself does not bear a CE mark but is part of a
product that complies with Directive 93/42/EEC concerning
medical devices. It is therefore covered by the power
wheelchair’s CE marking. See the power wheelchair’s
documentation for more information.
•
For information on electronics, see Invacare LiNX manuals. For
information on other electronics, see earlier revisions of service
manuals.
•
For information on other seating systems than the Modulite, see
corresponding service manuals or earlier revisions of service
manuals.
•
For specific settings, such as center of gravity adjustments, see
corresponding power wheelchair’s service manual.
1.2 General information
•
Service and maintenance work must be carried out taking this
service manual into account.
•
It is imperative that you observe safety information.
•
Information about operation or about general maintenance and
care work on the mobility device should be taken from the
operating manual.
• You can find information about ordering spare parts in the spare
parts catalogue.
•
Spare parts MUST match original Invacare parts. Only use spare
parts which have been approved by Invacare.
•
We reserve the right to make any alterations on the grounds of
technical improvements.
•
For more information about the product, for example product
safety notices and product recalls, contact your local Invacare
representative. For address and website see back page of this
manual.
•
The mobility device may only be maintained and overhauled by
qualified personnel.
•
The minimum requirement for service technicians is suitable
training, such as in the cycle or orthopedic mechanics fields, or
sufficiently long-term job experience.
– Experience in the use of electrical measuring equipment
(multimeters) is also a requirement.
– Special Invacare training is recommended.
•
Alterations to the mobility device which occur as a result of
incorrectly or improperly executed maintenance or overhaul
work lead to the exclusion of all liability on the side of
INVACARE.
•
If you have any problems or questions please contact Invacare
Service.
1.3 Notes on shipping
•
If the mobility device has to be shipped back to the manufacturer
for major repairs, you should always use the original packaging
for transport.
•
Please attach a precise description of the fault.
1.4 Symbols in this manual
In this manual, hazard statements are indicated by symbols. The
symbols are accompanied by a signal word that indicates the severity
of the risk.
WARNING
Indicates a hazardous situation that could result in
serious injury or death if it is not avoided.
CAUTION
Indicates a hazardous situation that could result in
minor or slight injury if it is not avoided.
IMPORTANT
Indicates a hazardous situation that could result in
damage to property if it is not avoided.
Gives useful tips, recommendations and information
for efficient, trouble-free use.
This product complies with Directive 93/42/EEC
concerning medical devices. The launch date of this
product is stated in the CE declaration of conformity.
Tools:
This symbol identifies a list of various tools,
components and items which you will need in order
to carry out certain work.
1.5 Images in this manual
The detailed images in this manual are given digits to identify
various components. Component numbers in text and operational
instructions always relate to the image directly above.
4 1604311-A