Codes; Introduction; Intended Use; Declaration Of Confomity - Mopedia RP701A Manual De Instrucciones

REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND
OF THE COUNCIL of 5 April 2017 concerning medical devices

1. CODES

RP701A Silver forearm crutch - Adult
RP701B Blue forearm crutch - Adult
RP701N Black forearm crutch - Adult
RP701R Red forearm crutch - Adult
RP701V Green forearm crutch - Adult

2. INTRODUCTION

Thank you for purchasing a MOPEDIA walking canes by Moretti S.p.A. This user 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 MOPEDIA by Moretti walking sticks are aids manipulated by one arm adapted to support and / or
help the mobility of people with mobility problems.
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 CONFOMITY

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 FOREARM CRUTCHES 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.
I Class Medical Device
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