S10/S12/S10A/S12A Patient Monitor User’s Manual
31
Class A equipment is intended to be used in industrial environment. Due to
conduction disturbance and radiation disturbance of this monitor, there may
be potential difficulties in ensuring electromagnetic compatibility in other
environments.
In addition to cables sold by the manufacturer of this monitor as spare parts
for internal components, the use of accessories and cables other than those
specified may result in increased emission or reduced immunity of this
monitor.
Even if other equipment meets the emission requirements of corresponding
national standards, this monitor may still be interfered by other equipment.
A warning that operation of the EQUIPMENT or SYSTEM below the
minimum amplitude or value may cause inaccurate results. The minimum
amplitude or value of patient physiological signal: the minimum amplitude of
ECG signal is 0.5mV, the minimum value of PR is 30bpm and the minimum
value of SpO2 is 70%.
Table 1
Guidance and manufacture’s declaration – electromagnetic emission
The monitor is intended for use in the environment specified below. The customer or the user of
the monitor should assure that it is used in such environment.
Emission test Compliance Electromagnetic environment - guidance
RF emissions
CISPR11
Group1 The monitor uses RF energy only for its internal
function. Therefore, its RF emissions are very low
and are not likely to cause any interference in
nearby electronic equipment.
RF emission
CISPR 11
Class A
The monitor is suitable for use in all establishments
other than domestic and those directly connected to
the public low-voltage power supply network that
supplies building used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations /
flicker emissions
IEC 61000-3-3
Complies
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