Mopedia RI840, Instruction Manual

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ENGLISH
I Class Medical Device
REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL
of 5 April 2017 concerning medical devices
1. CODES
RI840 - Electrical stand up lift max load 200 Kg with legs opening pedal
RI841 - Electrical stand up lift max load 200 Kg with legs opening lever
2. INTRODUCTION
Thank you for choosing a patient stand up lift MUEVO UP by MOPEDIA range, manufactured
by MORETTI S.p.A. Their design and quality are a guarantee of comfort, safety and reliability.
MUEVO UP by MOPEDIA 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 advices for your
safety. Please read carefully through the manual before using the patient lift/stand up. Should
you have any queries, please contact your retailer for advice and assistance.
3. INTENDED USE
Patient stand up lift MUEVO UP by MOPEDIA is intended to stand up and move people with
motor difficulties. An assistant operates the machine. The stand up lift cannot be used by one
person only.
If you should have any doubts please contact your dealer who will help and advice you correctly.
WARNING!
• Do not use the product for a purpose not indicated in this manual.
• Moretti S.P.A. declines all responsibilities for any consequences resulting from an
incorrect use of this product and from unauthorized alteration to the frame of the
product.
• The manufacturer reserves the right to change the information contained in this
document without previous notice.
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.
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.
To guarantee greater safety, Moretti SpA followed the EN ISO 10535:2006 guidelines relating
to lifters.