ARDEA ONE COMFY STEEL CP800-40, Instruction Manual

14

ENGLISH

I Class Medical Device

 according to Directive 93/42/EEC and 

further modifications

1. Codes

CP800-40 

Reclining wheelchair COMFY STEEL 40 cm 

CP800-43

Reclining wheelchair COMFY STELL 43 cm 

CP800-46

Reclining wheelchair COMFY STEEL 46 cm

2. Introduction

Thank  you  for  purchasing  comfy  steel  reclining  steel  reclining  wheelchair  ARDEA  ONE 
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 all parts for shipping damages and test before using. In case of damage, do not 

use the device. Contact your dealer for further instructions.

3. Intended use

This wheelchair is intended for people with mobility problems and can be used for self-pro-
pelling or with the aid of an operator. In all cases however it requires the intervention of an 
operator for the various adjustments you require.

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. EC declaration of conformity

Moretti S.p.A. hereby declares, under its own exclusive responsibility, that the products ma-
nufactured and sold by Moretti S.p.A. and belonging to the wheelchair category are compliant 
with the applicable provisions outlined in the Medical Devices Directive 93/42/EEC and fur-
ther 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 said 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