Mopedia MI190, Instruction Manual

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ENGLISH
Class I medical device
REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL
of 5 April 2017 on medical devices
1. CODES
MI190 Hydraulic bed lifting base
MI195 Electric bed lifting base
2. INTRODUCTION
Thank you for choosing a hospital bed lifting device in the MOPEDIA range by Moretti. The
MOPEDIA lifting bases by Moretti have been designed and constructed to satisfy all your needs
for practical, correct and safe use. This manual contains useful suggestions for using your
device properly and safely. Please read this manual in full before you use the lifting base you
have purchased. Should you have any queries, please contact your dealer for suitable advice
and assistance.
NOTE: Check to ensure that no parts of the product have been damaged during shipment.
Do not use the product if it is damaged and contact the retailer for further instructions.
WARNING!
• Do not use the product for any purpose other than that specified in this manual.
• Moretti S.p.A. declines any and all liability for damages resulting from improper
use of the device or any use other than that specified in this manual.
• The manufacturer reserves the right to modify the device and its relevant manual
without prior notice, in order to improve the product's features.
3. INTENDED USE
The MOPEDIA bed lifting bases are designed to support and adjust the height of the Moretti
MI100 – MI110 – MI120 hospital beds, in hospital and/or healthcare structures and entities
or at home.
4. EU DECLARATION OF CONFORMITY
MORETTI SpA declares, under its own exclusive responsibility, that the products made and
sold by MORETTI SpA in the BED ACCESSORIES product family conform with the applicable
provisions of Regulation (EU) 2017/745 of 5 April 2017 on MEDICAL DEVICES.
To this end, MORETTI SpA guarantees and declares as follows, under its own exclusive
responsibility:
1. The devices in question satisfy the general safety and performance requirements set out
in Annex I to Regulation (EU) 2017/745, as prescribed by Annex IV to said regulation.
2. The devices in question ARE NOT MEASUREMENT TOOLS.
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, in accordance with the
rules set out in Annex VIII to said regulation.
6. MORETTI SpA maintains and provides to the competent authorities, for at least ten years
from the date of manufacture of the last production lot, the technical documentation
proving conformity with Regulation (EU) 2017/745.
Note: The complete product codes, the manufacturer’s single registration number (SRN), the