Intended Use; Intended Environment - Etac immedia TurningMattress Instrucciones De Uso

General
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 user" in this user manual is the
person who is lying or sitting on the product. The carer or carers
are the people who manoeuvre the product.
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 user or carer.
The products comply with the standards applicable for Class 1
products in the European Council Directive MDD 93/42/EEC on
medical devices.
At Etac we strive to improve our products all the time and
therefore we reserve the right to make changes to products
without prior warning. All measurements given on illustrations
Symbols in general
Washing
Do not bleach
Tumbledry
Iron
Do not dryclean

Intended use

Regular turning and positioning of immobile users.

Intended environment

Acute care, Long-term care, Home care.
pH level
Wipe off
Never leave on the floor
Risk of sliding down
Keep out of the sun
4
and similar material are for guidance only and Etac cannot be
held liable for errors and defects.
The information given in this manual, including recommendations,
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 not be valid. If in doubt,
please contact Etac.
Warranty: Two-year warranty on material and manufacturing
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.
Read the user manual
Warning
Production year, month
and day
Batch no./Lot no.
User mass limit =
maximum rated load
The product can be
scrapped according to
national regulations
Manufacturer
Class 1 - European
Council Directive MDD
93/42/EEC on medical
devices