Codes; Introduction; Intended Use; Declaration Of Conformity - Mopedia RS825 Manual De Instrucciones

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

1. CODES

RS825 Foldable shower chair with backrest and wheels
RS826 Foldable shower chair with backrest
RS827 Bath bench without backrest
RS829 Bath bench with backrest
RS831 Bath bench U-shape without backrest
RS833 Bath bench U-shape with backrest
RS838 Shower chair with armrests
RS839 Shower chair with armrests and backrest
RS908 Toilet safety rails height adjustable and removable
RP770 Commode frame height adjustable

2. INTRODUCTION

Thank you for purchasing a MOPEDIA bath products by Moretti S.p.A. product range. 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. In case of doubts, we recommend to contact the dealer who can
help and advice you properly.
Note Check if any part has shipping damages and test before using. In case of damage, do
not use the device. 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.

3. INTENDED USE

The bath chair by Moretti is intended for disable patient assistance in bath tub.

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 SHOWER – BATHROOM CHAIRS 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.
I Class Medical Device
of 5 April 2017 concerning medical devices
3