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Invacare Revato H335 Manual Del Usuario página 3

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  • MEXICANO, página 18
1 General
1.1 Introduction
This user manual contains important information about the
handling of the product. To ensure safety when using the
product, read the user manual carefully and follow the safety
instructions.
Invacare reserves the right to alter product specifications
without further notice.
Before reading this document, make sure you have the latest
version. You find the latest version as a PDF on the Invacare
website.
If you find that the font size in the printed document is
difficult to read, you can download the PDF version from the
website. The PDF can then be scaled on screen to a font size
that is more comfortable for you.
In case of a serious incident with the product, you should
inform the manufacturer and the competent authority in
your country.
1.2 Warranty Information
We provide a manufacturer's warranty for the product
in accordance with our General Terms and Conditions of
Business in the respective countries.
Warranty claims can only be made through the provider from
whom the product was obtained.
1.3 Compliance
Quality is fundamental to the company's operation, working
within the disciplines of ISO 13485.
This product features the CE mark, in compliance with the
Medical Device Regulation 2017/745 Class I.
We are continuously working towards ensuring that the
company's impact on the environment, locally and globally, is
reduced to a minimum.
We only use REACH compliant materials and components.
Product-Specific Standards
The product meets the requirement of the standard DIN EN
12182 (Assistive products for persons with disability) and
related standards.
For further information about local standards and regulations,
contact your local Invacare representative. See addresses
at the end of this document.
1.4 Service life
The expected service life of this product is five years
when used daily in accordance with safety instructions and
intended use, stated in this manual. The effective service life
can vary according to frequency and intensity of use.
1.5 Limitation of Liability
Invacare accepts no liability for damage arising from:
Non-compliance with the user manual
Incorrect use
Natural wear and tear
Incorrect assembly or set-up by the purchaser or a third
party
Technical modifications
Unauthorised modifications and/or use of unsuitable
spare parts
1572997-G
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2 Safety
2.1 Safety Information
WARNING!
Risk of Serious Injury or Damage
Improper use of this product may cause injury
or damage.
– If you are unable to understand the warnings,
cautions or instructions, contact a health care
professional or provider before attempting to
use this equipment.
– Do not use this product or any available
optional equipment without first completely
reading and understanding these instructions
and any additional instructional material such
as user manual, service manual or instruction
sheet supplied with this product or optional
equipment.
WARNING!
Risk of Falling!
– Do not use if defective.
– Do not use as sports equipment or climbing aid.
– Do not make any unauthorised alterations or
modifications to the product.
WARNING!
Risk of Falling!
Excessive or intermittent loads can lead to
breaking.
– Do not exceed the maximum user weight, see 8
Technical Data, page 6 .
CAUTION!
Risk of Injury
Non-original or wrong parts may affect the
function and safety of the product.
– Only use original parts for the product in use.
– Due to regional differences, refer to your local
Invacare catalogue or website for available
options or contact your Invacare distributor. See
addresses at the end of this document.
2.2 Labels and Symbols on Product
Identification Label (Fig. 6)
Conformity mark
Lot number
Manufacturer
The identification label is attached to the bottom side
of the foldable grab bar.
3 Product Overview
3.1 Intended Use
Invacare Revato are grab bars made of rilsanized steel to be
installed on wall or floor with screws and can be flipped up.
Additional floor installation or a support leg are available to
increase stability.
Maximum safe
load
Read user
manual
Medical Device
3

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