4
ENGLISH
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 of production.
Note: Complete product codes, the manufacturer registration code (SRN), the UDI-DI code and any
references to used regulations are included in the EU declaration of conformity that Moretti S.p.A.
releases and makes available through its channels.
5. GENERAL WARNING
• DO NOT use this product or any available optional equipment without first completely
reading and understanding this instruction manual. If you are unable to understand the
warnings, cautions or instructions, contact a healthcare professional, dealer or technical
personnel before using this equipment otherwise injury or damage may occur.
• Consult your physician or therapist to determinate the correct adjustment and the correct
use of the wheelchair.
• Keep the packed wheelchair away from heat sources.
• SERVICE LIFE- the wheelchair limit usage is defined by the wear of non-replaceable parts.
• ALWAYS keep hands and fingers clear of moving parts to avoid injury.
• DO NOT allow children to play on or operate the wheelchair.
• Close the wheelchair as explained in this manual and lift it up from handles.
• DO NOT attempt to lift the wheelchair by any removable parts.
• The user and/or the patient will have to report any serious accident that have occurred
related the device to the manufacturer and appropriate authority of the State which the
user and/or patient belongs to.
6. SYMBOLS
Product code
Unique Device Identification
SN
Serial number
CE mark
EC
REP
0197
S N
Manufacturer
Batch Lot
Read the instruction manual
Medical Device
Conditions of disposal
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