Etac molift MRS Duo 2000 Manual De Usuario página 5

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
2-year warranty against defects in workmanship and materials of our products�
For Terms and conditions, see www�etac�com
Product identification
Product label
The Product label contain article number and
production date�
MRS Duo
SWL 300kg / 661lbs
Warning labels and Symbols
Symbols used on the product, explained in more
detail:
General
CE marked
Refer to user manual
Indoor Use only
Manufacturer
Date of manufacture
YYYY-MM-DD
Catalogue number
Serial number
Medical Device
5
Molift MRS Duo / www.etac.com
EN