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Idiomas disponibles
Idiomas disponibles
REGOLAMENTO (UE) 2017/745 DEL PARLAMENTO EUROPEO E DEL CONSIGLIO
1. CODE
RS900 Bath lift
2. INTRODUCTION
Thank you for purchasing the bath lift from the MOPEDIA line by MORETTI S.p.A. its design and
qualities guarantee comfort, safety and reliability to the user. The bath lift by MORETTI S.p.A.
has been designed to satisfy all your demands. This instruction manual contains advices and for
your safety and for a correct use of the aid. We recommend reading thoroughly the instruction
manual before using the bath lift. In case of doubts, contact your retailer.
3. INTENDED USE
The Moretti bath lift is intended for lowering and lifting a person in a bathtub.
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 BATH LIFTERS 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.
Dispositivo medico di classe I
del 5 aprile 2017 relativo ai dispositivi medici
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