Codes; Introduction; Intended Use; Declaration Of Conformity - Moretti Mopedia MUEVO Ri821 Manual De Instrucciones

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

1. CODES

HYDRAULIC LIFTS
RI821 HYDRAULIC actuator - payload 150 Kg - with pedal for legs opening
RI823 HYDRAULIC actuator - payload 150 Kg - with lever for legs opening
RI825 HYDRAULIC actuator - payload 180 Kg - with pedal for legs opening
RI827 HYDRAULIC actuator - payload 180 Kg - with lever for legs opening
ELECTRICAL LIFTS
RI822 ELECTRIC actuator - payload 150 Kg - with pedal for legs opening
RI824 ELECTRIC actuator - payload 150 Kg - with lever for legs opening
RI826 ELECTRIC actuator - payload 200 Kg - with pedal for legs opening
RI828 ELECTRIC actuator - payload 200 Kg - with lever for legs opening

2. INTRODUCTION

Thank you for choosing a patient lift/stand up lift from the MUEVO by MOPEDIA product
range by MORETTI S.p.A.. Their design and quality are a guarantee of comfort, safety and
reliability. MUEVO 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 by MOPEDIA patient lifts/stand up 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 above
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.
I Class Medical Device
of 5 April 2017 concerning medical devices
3