Mopedia RP145NC, Instruction Manual

3

ENGLISH

  I Class Medical Device

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

of 5 April 2017 concerning medical devices

1. CODES

1.1 Folding walking cane codes
RP145NC   Aluminum folding walking cane  with T-handle – Black  color   
RP145NL  Aluminum folding walking cane with T-handle – Black color  

1.2 Aluminum walking canes height adjustable codes
RP146 

Aluminum height adjustable walking cane T-handle - Black color  

RP148  

Aluminum height adjustable walking cane T-handle - Black color 

RP153D   Aluminum height adjustable walking cane anatomical right handle  
RP153S 

Aluminum height adjustable walking cane anatomical left handle  

2. INTRODUCTION

Thank you for purchasing a MOPEDIA walking canes  by 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 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 CONFORMITY

Moretti S.p.A. declares under its sole responsibility that the product made and traded by Mo-
retti S.p.A.and belonging to the group of WALKING STICKS 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.