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READ BEFORE USE
Read the user's guide completely before use and fully understand its content . Familiarize yourself with
the handling and functions of the product before use and practice them . Any caregiver that is going to
operate this chair should also read the user's guide in full .
You are responsible for the safety of the user . The safety of the user could be affected if you do
not follow the instructions in this user's guide . Nevertheless, not all possible circumstances and
unpredictable situations can be covered by this user's guide . Reason, care, and circumspection are
not features of the product; they are required of persons who use the product . If instructions are not
clear and further explanation is necessary, please contact your Convaid provider . If you do not follow
all instructions and warnings, serious injury or damage to the chair may occur . The latest version of all
instructions and product safety notices are available on the Convaid website (www .etac .us .com) and
can be printed in larger sizes . Additional video instructions are also available for reference purposes .
DEFINITION OF SYMBOLS
Indicates the need for the user to
consult the instructions for use for
important cautionary information such
as warnings and precautions that
cannot, for a variety of reasons, be
presented on the medical device itself .
Indicates a medical device that need
to be consulted with the instruction for
user
This symbol indicates potential fi nger
entrapment . .
This symbol indicates correct lifting
points for safe moving and handling .
This symbol indicates maximum user's
weight .
Indicates the manufacturer's serial
number so that a specifi c medical
device can be identifi ed.
CONVAID USER'S GUIDE
This symbol is a mandatory marking
for devices entering the European
market to indicate conformity
with the essential health and
safety requirements set out in
European Directives . The symbol
may be accompanied by a four-digit
identifi cation number of the notifi ed
body . The vertical dimensions may
not be less than 5 mm high .
Indicates the Authorized
representative in the European
Community .
This symbol indicates the
manufacturer's catalogue number
so that the medical device can be
identifi ed.
Indicates the medical device
manufacturer .
Indicates the date when the medical
device was manufactured .
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