3
ENGLISH
I Class Medical Device
REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5
April 2017 concerning medical devices
1.
CODES
CR500-1
Telescopic ramps 152 cm - PAIR
CR500-2
Telescopic ramps 213 cm - PAIR
CR503-1
F
oldable ramp 61 cm
CR503-2
Foldable ramp 213 cm
CR505-1
Tri-folding ramp 152 cm
CR505-2
Tri-folding ramp 183 cm
CR505-3
Tri-folding ramp 213 cm
CR507-1
F
ixed ramps 61 cm - PAIR
CR507-2
Fixed ramps 183 cm - PAIR
CR509-1
Platform ramp 61 cm
CR509-2
Platform ramp 91 cm
CR509-3
Platform ramp 122 cm
2.
INTRODUCTION
Thank you for purchasing an ARDEA ramp by Moretti S.p.A. product range.This user’s manual
provi-des some suggestions as how to correctly use the product you have chosen and gives some
valuab-le 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 damage and test before using. In case of damage, do not use
the device. Contact your dealer for further instruction.
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 notice.
3. INTENDED USE
This ramp is intended for the removal of architectural barriers for persons with mobility diffi-
culties and must be used with the assistance of an operator.
4. DECLARATION OF CONFORMITY
Moretti S.p.A. declares under its sole responsibility that the product made and traded by Moretti
S.p.A.and belonging to the group of RAMPS – ARDEA complies with the provisions of the regulation
2017/745 on MEDICAL DEVICES of 5 April 2017.
For this purpose, Moretti S.p.A. guarantees and declares under its sole responsibility what follows:
1. The devices satisfy the requirements of general safety and performance requested by the
Annex I of regulation 2017/745 as laid down by the Annex IV of the above mentioned regulation.
2. The devices ARE NOT MEASURING INSTRUMENTS.
3. The devices ARE NOT MADE FOR CLINICAL TESTS.
4. The devices are packed in NON-STERILE BOX.
5. The devices belong to class I in accordance with the provisions of Annex VIII of the above
mentioned regulation.
6. Moretti S.p.A. provides to the Competent Authorities the technical documentation to prove
the conformity to the 2017/745 regulation, for at least 10 years from the last lot production.
