Mindray BeneView T8, Operation Manual

Page: 257 / 290

B-1
B
EMC
The patient monitor meets the requirements of IEC 60601-1-2:2001
Note
z
Using accessories, transducers and cables other than those specified may result in
increased electromagnetic emission or decreased electromagnetic immunity of the
patient monitoring equipment.
z
The patient monitor or its components should not be used adjacent to or stacked
with other equipment. If adjacent or stacked use is necessary, the patient monitor
or its components should be observed to verify normal operation in the
configuration in which it will be used.
z
The patient monitor needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information provided below.
z
Other devices may affect this monitor even though they meet the requirements of
CISPR.
z
When the inputted signal is below the minimum amplitude provided in technical
specifications, erroneous measurements could result.
Guidance and Declaration - Electromagnetic Emissions
The patient monitor is suitable for use in the electromagnetic environment specified below. The
customer or the user of the patient monitor should assure that it is used in such an environment.
Emission tests Compliance Electromagnetic environment - guidance
Radio frequency (RF)
emissions CISPR 11 Group 1 The patient 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 emissions CISPR 11 Class A
Harmonic emissions
IEC61000-3-2
Class A
Voltage
fluctuations/flicker
emissions
IEC61000-3-3 Compliance
The patient monitor is suitable for use in all
establishments other than domestic and those
indirectly connected to the public low-voltage power
supply network that supplies buildings used for
domestic purposes.