Etac Pediturn, Руководство пользователя

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General
Features
Pediturn is a slim, lightweight turnplate for floor use
in connection with manual handling in the standing or
seated position, where the client must rotate but is not
capable of moving his/her legs without assistance.
Thank you for choosing an Etac product.
To avoid accidents and injury when moving and handling
the products, read the manual carefully.
The person described as "the client" in this user manual is
the person who rests his/her feet or stands on the prod-
uct. The carer or carers are the people who manoeuvre the
product.
The products comply with the standards applicable for
Class 1 products in the European Council Directive
MDD 93/42/EEC on medical devices.
This symbol appears alongside the text in
the manual. It draws the reader's attention
to points at which there may be a risk to the
health and safety of the client or carer.
At Etac we strive to improve our products all the time and
therefore we reserve the right to make changes to prod-
ucts without prior warning. All measurements given on
illustrations and similar material are for guidance only and
Etac cannot be held liable for errors and defects.
The information given in this manual, including recom-
mendations, combinations and sizing, does not apply to
special orders and modifications. If the customer makes
adjustments, repairs or combinations not predetermined
by Etac, the Etac CE certification and Etac warranty will
be voided. If in doubt, please contact Etac.
Warranty: Two-year warranty on material and manufac-
turing defects, provided that the product is used correctly.
For further information on the Etac transfer range, see
www.etac.com.
The product can be scrapped in accordance with national
regulations.
Washing
Handwash
Wipe off
Tumbledry
Iron
Do not dryclean
Do not bleach
Risk of sliding down
Never leave on the floor
Warning
Read the User Manual
Batch no./Lot no.
Max. weight
The product can be
scrapped in accordance
with national regulations
Manufacturer
Class 1 - European Council
Directive MDD 93/42/EEC
on medical devices