4
ENGLISH
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
WARNING!
Always pay close attention to the presence of moving parts that could cause limb
entrapment and injury.
• For proper use of the device refer to this manual, checking with a particular attention at
the warnings before use.
• For proper use of the device to consult your doctor or therapist.
• Keep the packaged product away from any source of heat because the packaging is made
of cardboard.
• The useful life of the accessory is determined by wear of parts that cannot be repaired
and/or replaced.
• Be careful when children are nearby.
• Do not exceed the maximum payload.
• 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
CE mark
EC
REP
0197
S N
Manufacturer
Batch Lot
Read the instruction manual
Medical Device
Conditions of disposal
EC
REP
0197
S N
Attention, should read the instructions
Production dates
EC
REP
0197
S N
Waste Electrical & Electronic Equipment (WEEE)
Protection against dust and water splashes
B Type
Содержание MUEVO
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