SAFETY
4 Model 3000T Operation Manual
CAUTION: Portable and mobile RF communications equipment can affect medical electrical equipment.
WARNING: The Model 3000T should not be used adjacent to or stacked with other equipment, however if
adjacent or stacked use is necessary, the Model 3000T should be observed to verify normal operation in the
configuration in which it will used.
Accessories
WARNING: The use of accessories other than those specified below may result in increased emissions or
decreased immunity of the equipment.
Ivy P/N Description
590323 Low noise, three lead ECG patient cable (US)
590318 Set of three radiotranslucent lead wires (US)
590381 Low noise, three lead ECG patient cable (EU)
590376 Set of three radiotranslucent lead wires (EU)
590342 Radiotranslucent ECG electrodes
Signal Amplitude
WARNING: The minimum patient physiological “R-wave” signal amplitude is 0.5 mV (AAMI EC-13 3.2.6.1).
The use of the Model 3000T, below the above amplitude value, may cause inaccurate results:
Guidance and manufacturer’s declaration – Electromagnetic emissions
The Model 3000T monitor is intended for use in the electromagnetic environment specified below.
The customer or the user of the Model 3000T should insure that they are used in such an
environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1 The Model 3000T uses RF energy only for its
internal function. Therefore, their RF emissions are
very low and are not likely to cause any interference
in nearby electronic equipment.
RF emissions
CISPR 11
Class A The Model 3000T is suitable for use in all
establishments other than domestic and those
directly connected to the public low-voltage power
supply network that supplies buildings 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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