Etac Molift Air Tilt, Руководство пользователя

Страница: 4 / 64

Molift Air Tilt / www.etac.com
1
Important
This User Manual contains important safety instructions and
information regarding the use of the sling and accessories.
In this manual the client is the person being lifted.
The caregiver is the person operating the hoist.
This symbol indicates important information
related to safety. Follow these instructions
carefully.
Read User Manual before use!
It is important to fully understand the con-
tent of the user manual before attempting to
use the equipment.
Visit www.etac.com for download of documentation to ensure
you have the latest version.
General
Conditions for Use
Lift and transfer of a client will always pose a certain risk and
only trained personnel are allowed to use the equipment and
accessories covered by this user manual. The rail system must
be installed by certified personnel in accordance with applicable
installation instructions.
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.
The hoist is not intended to be operated by the client being lifted.
If a hoist is to be used by a client living on their own, then some
form of communication device shall be installed in the area of use
of the hoist so that in the event of an emergency the client is able
to summon assistance. This may, for example, be the fitting of an
alarm system or the supply of a conveniently placed telephone,
etc.
Only certified personnel are allowed to open
hoist or accessories to perform service or
repair. Risk of injury from rotating parts and
electric shock.
Warranty notice
Two-year warranty against defects in work-
manship and materials of our products.
One-year warranty for batteries.
Please refer to www.etac.com for terms and
conditions.
CE declaration
The product, and its related accesso-
ries, 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 has been tested and ap-
proved 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 manufacturer and the
competent authority of the Member
State in which the user and/or patient
is established.