Etac Molift MRS Quattro Посібник з монтажу - Сторінка 4

Переглянути онлайн або завантажити pdf Посібник з монтажу для Допомога з мобільності Etac Molift MRS Quattro. Etac Molift MRS Quattro 16 сторінок.

Molift MRS Quattro / 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.

Hoisting and transferring a person may contain an element of risk. A risk assessment should be carried

out prior to use and only trained personnel should use the equipment as described in the 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.

Only suitable trained people should install this equipment.

The work contains handling of heavy loads.

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 label

The Product label contain article number and

production date.

MRS Quattro

SWL 300kg / 661lbs

Warnng 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