Codes; Introduction; Intended Use; Declaration Of Conformity - Mopedia RI900 Manual De Instrucciones

REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL

1. CODES

RI900 - Electrical lift Muevo Home – payload 135 Kg

2. INTRODUCTION

Thank you for choosing a patient lift and transfer device from the MUEVO HOME by MOPEDIA
product range by MORETTI S.p.A.. Their design and quality are a guarantee of comfort, safety
and reliability. MUEVO HOME by MOPEDIA patient lifts/stand up lifts by MORETTI S.p.A. are
designed and built to meet all your demands for a practical, correct use. This user manual
provides for some suggestions as to how correctly use the lift you have chosen and offers a
lots of valuable advice for your safety. Please read carefully through the manual before using
the patient lift/stand up lift. Should you have any queries, please contact your retailer for
advice and assistance.

3. INTENDED USE

MUEVO HOME by MOPEDIA patient lifts are intended to lift and move people with motor
difficulties. An assistant operates the machine. The lifts cannot be used by only one person.
MORETTI S.p.A. refuses all liability for damages caused by improper use of the device or by its
use for a purpose other than that one specified in this manual.

4. DECLARATION OF CONFORMITY

Moretti S.p.A. declares under its sole responsibility that the product made and traded by Moretti
S.p.A.and belonging to the group of PATIENT LIFTS MOPEDIA complies with the provisions of
the regulation 2017/745 on MEDICAL DEVICES of 5 April 2017.
For this purpose, Moretti S.p.A. guarantees and declares under its sole responsibility what
follows:
1. The devices satisfy the requirements of general safety and performance requested by the
Annex I of regulation 2017/745 as laid down by the Annex IV of the above mentioned regulation.
2. The devices ARE NOT MEASURING INSTRUMENTS.
3. The devices ARE NOT MADE FOR CLINICAL TESTS.
4. The devices are packed in NON-STERILE BOX.
5. The devices belong to class I in accordance with the provisions of Annex VIII of the abov
mentioned regulation
6. Moretti S.p.A. provides to the Competent Authorities the technical documentation to prove
the conformity to the 2017/745 regulation, for at least 10 years from the last lot production
Note: Complete product codes, the manufacturer registration code (SRN), the UDI-DI code
and any references to used regulations are included in the EU declaration of conformity that
Moretti S.p.A. releases and makes available through its channels
I Class Medical Device
of 5 April 2017 concerning medical devices
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