Electromagnetic Compatibility Information - Hartmann Thermoval baby 925 091 Mode D'emploi

Electromagnetic Compatibility Information

The Thermoval baby infrared fever thermometer is intended for use in one of the electromagnetic environments specified below (see Table 1–3). The customer or user of the Thermoval baby
should assure that it is used in such an environment.
Table 1
For all MEDICAL-ELECTRICAL (ME) DEVICES and ME SYSTEMS: Guidance and Manufacturer's Declaration – Electromagnetic emissions
Emissions test
RF emissions CISPR 11
RF emissions CISPR 11
Harmonic emissions IEC 61000-3-2
Voltage fluctuations/flicker emissions
IEC 61000-3-3
Table 2
For all MEDICAL-ELECTRICAL (ME) DEVICES and ME SYSTEMS: Manufacturer declaration and guidance – Electromagnetic immunity
Immunity test IEC 60601 test level
Electrostatic discharge (ESD) ± 6 kV / 8 kV contact
IEC 61000-4-2 ± 8 kV / 15 kV air
Power frequency (50/60 Hz) 3 A/m
magnetic field IEC 61000-4-8 30 A/m
Compliance Electromagnetic environment – guidance
The Thermoval baby uses RF energy only for its internal function.
Group 1
Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.
The Thermoval baby is suitable for use in all establishments, including domestic establishments and those directly
Class B
connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.
N/A
N/A
Compliance level
± 6 kV / 8 kV contact
± 8 kV / 15 kV air
3 A/m
30 A/m
Electromagnetic environment – guidance
Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material,
the relative humidity should be at least 30 %.
Power frequency magnetic fields should be at levels characteristic of a typical location in a
typical commercial or hospital environment.
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