Etac Molift Mover 300 L Gebruikershandleiding - Pagina 6
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Molift Smart 300 L / 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.
The product is manufactured and tested 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
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 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
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.
Mover 300 L
Gross weight 340kg / 750lbs
SWL 300kg / 661lbs
26.4V DC, IP24
Duty cycle 10%
General
Warning labels and symbols
Symbols used on the product, explained in more
detail:
Type BF applied part
CE marked
Refer to user manual
Indoor use only
Do not dispose in
general waste
Emergency lowering
Service indicator
6
Battery indicator
Manufacturer
Date of manufacture
YYYY-MM-DD
Catalogue number
Serial number
Medical Device