Before Using This Product, Read This Manual And Save For; General; Information About The User Manual; Symbols In This Manual - Küschall R33 Manual Del Usuario

1 GENERAL

1.1 Information about the User Manual

Thank you for choosing a küschall
This User Manual contains important information about
using the wheelchair. In order to ensure safety when using
your wheelchair, read the User Manual carefully and follow
the safety information.
If your vision is impaired, you can view the user manual
as a PDF file on the Internet at www.kuschall.com and
enlarge it on-screen as required. If you cannot enlarge the
text and graphics sufficiently, please contact the küschall
distributor for your country;
Refer to addresses on the reverse of this document. If
necessary, we will provide you with a high resolution PDF
file of the user manual. Moreover, you can have the PDF
file read out to you with the aid of suitable programs using
special language functions on your computer (e.g. in
Adobe ® Reader ® X: Shift+Ctrl+Y).
The equipment of your wheelchair may differ from
the descriptions and diagrams given here due to
the wide range of models available.
For latest important product information (e.g.: product
safety notices, product recalls, ...) please refer to our
website at www.kuschall.com, your local specialized
dealer or contact Invacare
see back page of this manual).
1583557-D
® wheelchair.
® in your country (for addresses,

1.2 Symbols in this manual

In this User Manual warnings are indicated by symbols.
The warning symbols are accompanied by a heading that
indicates the severity of the danger.
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.
Manufacturer
General
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