11
ENGLISH
I Class Medical Device according to Directive93/42/EEC
and further modifications
1. CODES
RS831
Bath bench u-shape without backrest
RS833
Bath bench u-shape with backrest
RS838
Shower chair with armerst and without backrest
RS839
Shower chair with armerst and backrest
RS908
Toilet safety rails painted steel height adjustable and removable
RP770
Commode frame in painted aluminum, 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.
3. INTENDED USE
The bath chair by Moretti is intended for disable patient assistance in bath tub
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. EC DECLARATION OF CONFORMITY
Moretti S.p.A. hereby declares, under its own exclusive responsibility, that the products
manufactured and sold by Moretti S.p.A. and belonging to the bath aids category are in com-
pliance with the applicable provisions outlined in the Medical Devices Directive 93/42/EEC
and further modifications.
To this end Moretti S.p.A. guarantees and declares as follows, under its own responsibility:
1. The devices in question satisfy the essential requirements of Annex I of directive 93/42/
EEC as prescribed by Annex VII of the above directive
2. A complete list of the concerned devices in mentioned in the enclosure A of the declaration
3. The devices in question ARE NOT MEASUREMENT DEVICES
4. The devices in question ARE NOT INTENDED FOR CLINICAL INVESTIGATION
5. The devices in question are sold in NON STERILE packing
6. The devices in question should be considered as belonging to class I
7. DO NOT use/install the devices in question for any other purpose than that expressly
indicated by Moretti S.p.A.
8. Moretti S.p.A. maintains and submits the documentation certifying conformity with
Directive 93/42/EEC to the proper authorities and further modifications
