Service Manual – 5 / 63
XE_ABS_MT_AN_200224
4. ABSOLU TECHNICAL SPECIFICATIONS
4.1. Classification
The system is intended for continuous operation and has the following classification:
B (protection against electrical shocks)
IP20 (protection from solid substances > 12,5mm)
4.2. Electrical requirements
Maximum power consumption
WARNINGS
Only mount/use on the ABSOLU module the power supply bloc approved by QUANTEL
MEDICAL (please refer to the table above for specifications details).
To avoid any risk of electric shock, this equipment must only be connected to supply mains
with protective earth.
4.3. Compliance
Medical electrical equipment-Part 1: General requirements for basic safety
and essential performance
Medical electrical equipment-Part 1: General requirements for basic safety
and essential performance – Amendment electromagnetic compatibility –
requirements and testing
Medical electrical equipment-Part 1-6: General requirements for basic
safety and essential performance – Amendment: usability
Medical devices – Application of usability engineering to medical devices
Medical device software – Software life-cycle process (IEC 62A/474/CDV)
Medical devices – Application of risk management to medical devices
(ISO/DIS 14971)
European Medical Device Directive
WARNING
Precautions to take with other devices using power supplies: the ABSOLU conforms to IEC
standard 60 601-1 (electric compatibility). All the other devices used in conjunction with the
ABSOLU must be conformed to this standard.
CAUTION
Precautions to take to avoid electromagnetic interferences with other devices: the ABSOLU
conforms to IEC standard 60 601-1-2 (electromagnetic compatibility). Make sure that all other
devices used in the same room are in accordance with this standard.
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