4
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 WARNINGS
• For correct use of the device, carefully refer to the following manual
• For correct use of the device always consult your doctor or therapist
• Keep the packaged product away from any source of heat as the packaging it is made of
cardboard
• The useful life of the device is determined by the wear of non-repairable and / or replaceable
parts
• Always pay close attention to the presence of moving parts which could cause limb entrapment
and personal injury
• Always pay attention to the presence of children
• Do not lift the wheelchair by removable parts which could accidentally come off during lifting
• The user and / or the patient must report any serious accident occurring in relation to the device
to the manufacturer and to the competent authority of the State in which the user and / or the
patient is established.
6. SYMBOLS
Product code
S N
Unique Device Identification
CE mark
0197
Manufacturer
Batch Lot
EC
REP
Read the instruction manual
Medical Device
Conditions of disposal
Serial Number