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Idiomas disponibles
Idiomas disponibles
REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL
1. CODES
RP780:
4 in 1 functions commode chair
RP781:
4 in 1 functions foldable commode chair
RP782:
4 in 1 functions commode chair with castors
RP783:
4 in 1 functions commode chair with foldable armrests
2. INTRODUCTION
Thank you for purchasing a MOPEDIA multifunction chairs for bathroom Moretti S.p.A. This user's
manual provides some suggestions as how to correctly use the product you have chosen and gives
some valuable advice for your safety. Please read through the manual carefully before using the
product. Should you have any queries, please contact your retailer for advice and assistance.
3. INTENDED USE
The multifunction chairs for bathroom MOPEDIA by Moretti are intended to be used as an aid in
shower and bathroom for people with walking difficulties. They include four functions in one: a
stabilizer for water rise, support for water, commode chair and shower seat.
CAUTION!
• 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 SEAT AND SUPPORT FOR WC 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 Moret-
ti 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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