Moretti EASYRED EM101, Instruction Manual

9

ENGLISH

I Class Medical Device

according to Directive 93/42/EEC and further modifications

1. Code

EM101

 SCOOP STRATCHER 

2. Introduction

Thank you for purchasing a EASYRED by Moretti S.p.A. device. Made of aluminum alloy material. 
separable rigid structure, with clutch devices at both ends, the stretcher can be separated into 
right and left 2 parts, no need to move the patient's at original place, the patients can be quickly 
shovel into or out from under the body, reduce secondary injury to the patients. Widely used in 
hospital,  ambulance  and  sports  environments.  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

Rescue device for the transport and transfer of injured.

WARNINGS!
•  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 manufactu-
red and sold by Moretti S.p.A. and belonging to the cane aids  category are in compliance 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. The devices in question ARE NOT MEASUREMENT DEVICES
3. The devices in question ARE NOT INTENDED FOR CLINICAL INVESTIGATION
4. The devices in question are sold in NON STERILE packing
5. The devices in question should be considered as belonging to class I
6. DO NOT use/install the devices in question for any other purpose than that expressly indicated 
by Moretti S.p.A.
7. Moretti S.p.A. maintains and submits the documentation certifying conformity with
  Directive 93/42/EEC to the proper authorities and further modifications

5. General warnings

•  READ carefully the entire manual before using the device .
•  The product should be used only by qualified personnel
•  Make sure that the product is delivered complete and keep it packed away from heat sources
•  SERVICE LIFE- the device use limit is defined by the wear of the parts
•  Store in a dry place
•  DO NOT allow children to play or operate the device