Codes; Introduction; Intended Use; Declaration Of Conformity - Mopedia MI094 Manual De Instrucciones

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

1. CODES

MI094 - Patient lift for beds with headboard (Tulipano type)
MI095 - Patient lift for beds with headboard (Ibisco type)
MI096 - Aluminium I.V. Poles with 2 Plastic Hooks for beds (Ibisco Type)
MI097 - Universal patient lift with base

2. INTRODUCTION

Thank you for choosing a patient lift by MOPEDIA range, manufacturer by MORETTI S.p.A.
Their design and quality are a guarantee of comfort, safety and reliability. Patient lift 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 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. Should you have any queries, please contact
your retailer for advice and assistance.

3. INTENDED USE

Mopedia Patient Lifts poles (MI094-MI095-MI097)are designed for people in hospital or at
home who have difficulties to sit or lie down on a bed.
The I.V. Poles for hypodermoclysis MOPEDIA (MI096) is a support device medical and health
activities during administration to the patient of intravenous fluids.
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.
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 ACCESSORIES FOR BEDS complies with the provi-
sions 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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