Product Identification - Etac Molift Partner 255 Manual De Usuario

Molift Partner 255 / www.etac.com
CE declaration
The product, and its related accessories, described in this instruction for use (IFU), is in com-
pliance with the regulation (EU) 2017/745 of 5. April 2017 – as a medical device, risk class I.
The product has been tested and approved by a third party according to standards IEC
60601-1, IEC 60601-1-2 and EN/ISO 10535:2006.
Any serious incident that occurs in relation to the device should be reported to the manu-
facturer 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 open lifter or accessories to perform service
or repair. Risk of injury from rotating parts and electric shock.
The lifter is not intended to be operated by the person being lifted.
Warranty notice
Two-year warranty against defects in workmanship and materials of our products.
One-year warranty for batteries.
Please refer to www.etac.com for terms and conditions.

Product identification

Product label
The Product labels barcode contain article number,
serial number and production date.
Partner 255
Gross weight 298kg / 657lbs
SWL 255kg / 562lbs
26.4V DC, IP24
Duty cycle 10%
Warning labels and Symbols
Symbols used on the product, explained in more
detail:
General
60601-1
Type BF applied part
CE marked
Refer to user manual
Indoor use only
Do not dispose in
general waste
Emergency lowering
Service light
6
Battery light
Certification body mark
60601-1
Manufacturer
Date of manufacture
YYYY-MM-DD
Catalogue number
Serial number
Medical Device