4
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.
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 Moret-
ti S.p.A. releases and makes available through its channels.
4.1 Standards and guidelines reference
Safety tests required by UNI EN 12182
5. GENERAL WARNINGS
• 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.
• For proper use of the device consult your doctor or therapist.
• Keep the packaged product away from any source of heat because the packaging is made
of cardboard.
• The shelf-life of the accessory is determined by the wear of parts that cannot be repaired
and/or replaced.
• Be careful when children are nearby.
• Do not exceed the maximum payload.
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