Codes; Introduction; Intended Use; Declaration Of Conformity - Moretti MOPEDIA RS992X Manual De Instrucciones

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

1. CODES

RS992X – Overbed table with wheels, painted steel frame, manual regulation
RS997X – Overbed table with wheels, painted steel frame, automatic regulation

2. INTRODUCTION

hank you for choosing an overbed table by MOPEDIA range, manufacturer by MORETTI
S.p.A. Their design and quality are a guarantee of comfort, safety and reliability. Overbed
tables by MOPEDIA by MORETTI S.p.A. are designed and built to meet all your demands
for a practical, correct use. This user manual provides some suggestions to correctly use
the tables you have chosen and offers a lot of valuable advice for your safety. Please read
carefully through the manual before using the overbed table. Should you have any queries,
please contact your retailer for advice and assistance.

3. INTENDED USE

The MOPEDIA bed trays are primarily intended for people who have mobility problems,
mainly bedridden where it is expected the consumption of meals in bed or chair. However
they are adaptable both in hospitals and home.
NOTE:
Check that the product has not been damaged during shipment. In case of damage do not
use it and contact your dealer for further instructions.
• 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 groups of BEDS TABLE 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
I Class Medical Device
of 5 April 2017 concerning medical devices
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