A-1
A Product Specifications
A.1 Classifications
The patient monitor is classified, according to IEC60601-1:
Type of protection against electrical shock
Class I, equipment energized from an external and internal electrical
power source.
Degree of protection against electrical shock
Type BF defibrillation proof for CO2 monitoring
Type CF defibrillation proof for ECG, RESP, TEMP, SpO2, NIBP, IBP, and
CCO.
Mode of operation
Continuous
Degree of protection against harmful ingress
of water
Main unit: IPX2 (Protected against vertically falling water drops when
ENCLOSURE tilted up to 15°)
T1 docking station, handle: IPX1 (Protected against vertically falling
water drops)
Degree of protection against hazards of
explosion
Not suitable: Equipment not suitable for use in the presence of a
flammable anesthetic mixture with air with oxygen or nitrous oxide.
A.2 Environmental Specifications
WARNING
The equipment may not meet the performance specifications if stored or used outside the specified
temperature and humidity ranges.
Main unit
Item Operating conditions Storage conditions
Temperature (℃)
0 to 40 -30 to 70
Relative humidity (noncondensing) 15% to 95% 10% to 95%
Barometric (kPa) 57.0 to 107.4 16.0 to 107.4
Microstream CO
2
module
Item Operating conditions Storage conditions
Temperature (℃)
0 to 40 -20 to 60
Relative humidity (noncondensing) 15% to 95% 10% to 95%
Barometric (mmHg) 57.3 to 105.3 57.3 to 105.3
Sidestream CO
2
module
Item Operating conditions Storage conditions
Temperature (℃)
5 to 40 -20 to 60
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