4
ENGLISH
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
Unique Device Identification
CE mark
EC
REP
0197
S N
Manufacturer
Batch Lot
Read the instruction manual
Medical Device
Conditions of disposal
Summary of Contents for RS992 Series
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Page 13: ...MA RS992 RS997 02 A_ENG_10 2020 OVERBED TABLES INSTRUCTION MANUAL ENGLISH ...
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Page 25: ...MA RS992 rs997 02 A_ESP_10 2020 MESITAS AUXILIARES DE CAMA MANUAL DE INSTRUCCIONES ESPAÑOL ...