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

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

1. CODES

RP682 2-wheel steel foldable rollator with seat NETTUNO

2. INTRODUCTION

Thank you for choosing a MOPEDIA range rollators by Moretti S.p.A. MOPEDIA range rollators
manufactured by Moretti S.p.A. are designed to satisfy all your requirements for practical, correct
and safe use. This manual provides some useful suggestions for correctly using the device you
have selected and offers valuable advice for your safety. We recommend reading the entire
manual carefully before using the rollator you have purchased. Should you have any queries,
please contact your retailer for proper advice or assistance.

3.INTENDED USE

This rollator fit for people with movement problems. Can be used as assistance to facilitate
ambulation or even servo-assisted ambulatory. Anyway, it can't be used by people with evident
malfunction of the hand or the arm, even by people with balance problems. The rollator can be
used inward and outward. We recommend using on flat surface where the wheels can reach the
land. It can't be used on rock ground or on slanted area as the rollator can be unstable. The device
is not intended to carry people or things.
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 ROLLATORS 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.
I Class Medical Device
of 5 April 2017 concerning medical devices
3