Idiomas disponibles
Idiomas disponibles
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
Moretti S.p.A. releases and makes available through its channels.
5. GENERAL WARNINGS
• For proper use of the device refer to this manual
• Keep the packaged product away from any source of heat because the packaging is made of
paper
• The shelf-life of the accessory is determined by wear of parts cannot be repaired and/or
replaced
• Be careful when children are nearby
• Do not exceed the max payload on the shelves shown in this manual to prevent deformation and
breakage
• Before using the device, always check that the assembly screws are well tight
• 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
S N
Unique Device Identification
CE mark
0197
Manufacturer
EC
REP
Batch Lot
Read the instruction manual
Medical Device
Conditions of disposal
