Molift MRS Duo Flex / www.etac.com
CE declaration
The product, and its related accessories, described in this instruction for use (IFU), is in compliance
with the regulation (EU) 2017/745 of 5. April 2017 – as a medical device, risk class I.
Any serious incident that occurs in relation to the device should be reported to the manufacturer
and the competent authority of the Member State in which the user and/or patient is established.
Conditions for Use
Lift and transfer of a person will always pose a certain risk and only trained personnel are allowed to use
the equipment and accessories covered by this user manual.
Modifications and use of components made by other manufacturers.
We recommend only using Molift components and spare parts. Declaration of conformity is not valid
and Etac is not responsible for warranty if any modifications are made to the product. Etac shall not be
liable for faults or accidents that can occur when using components made by other manufacturers.
Only certified personnel are allowed to perform repairs.
Warranty notice
Two-year warranty against defects in workmanship and materials of our products.
Please refer to www.etac.com for terms and conditions.
Product identification
Product label (example)
The Product label contains article number, max
width, mounted trolley and safe working load.
MRS Duo Flex
SWL 275kg / 606lbs
General
Warning labels and Symbols
Symbols used on the product, explained in more
detail:
Refer to user manual
Indoor Use only
Manufacturer
Date of manufacture
YYYY-MM-DD
Catalogue number
Serial number
Medical Device
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