ARDEA ONE COMFY STEEL CP800-40, Инструкция по эксплуатации

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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