ENGLISH
13
I Class medical device,
according Directive 93/42/EEC and subsequent amendments
1. CODES
MO411A
Aluminum ward screen with 3 panels
MO412C
Chromed steel ward screen with 3 panels
MO414C
Chromed steel ward screen with 4 panels
MO415A
Aluminum ward screen with 4 panels
2. INTRODUCTION
Thank you for choosing a metal ward screen from the SKEMAFORM by MORETTI S.p.A. Their
design and quality are a guarantee of comfort, safety and reliability. The metal ward screens
from the SKEMAFORM by MORETTI S.p.A. are designed and built to meet all your demands for
a practical and correct use. This user manual provides for some suggestions as how to use the
item you have chosen correctly and offers a lots of valuable advices for your safety. Please read
carefully this manual before using the metal ward screen. Should you have any queries, please
contact your retailer for advice and assistance.
3. INTENDED USE
The metal ward screen by SKEMAFORM is a device formed by 3 or 4 panels linked together by
zippers, intended and used as a mobile or partition wall.
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 EC 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 WARD SCREEN category are
compliant with the applicable provisions outlined in the Medical Devices Directive 93/42/EEC:
To this aim 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 mentioned directive.
2. The complete list of the devices in question is available in annex.
3. The devices in question are not measurement tools.
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 one expressly
indicated by MORETTI S.P.A.
8. Moretti S.P.A. maintains and submits the technical documentation certifying the conformity
of the products in question with the directive 93/42/eec to the proper authorities
