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41
G EMC Test Results
Guidance and manufactu
rer’s declaration-electromagnetic emissions for
all EQUIPMENT and SYSTEMS
Guidance and manufacturer’s declaration-electromagnetic emission
The iAED-S1 Automated External Defibrillator is intended for use in the
electromagnetic environment specified below. The user of the iAED-S1
Automated External Defibrillator should assure that it is used in such
environment.
Emissions test Compliance Electromagnetic environment-guidance
RF emissions
CISPR 11
Group 1
The iAED-S1 Automated External
Defibrillator uses RF energy only for its
internal function. Therefore, its RF
emissions are very low and not likely to
cause any interference in nearby
electronic equipment.
RF emissions
CISPR 11
Class B
The iAED-S1 Automated External
Defibrillator is suitable for using in all
establishments including domestic
establishments and those directly
connected to a low voltage power
supply network which supplies buildings
used for domestic purposes.
Harmonic
emissions
IEC 61000-3-2
N/A
Voltage
fluctuations/
flicker
emissions
IEC 61000-3-3
N/A
Guidance and manufacturer’s declaration-electromagnetic immunity-for
all EQUIPMENT and SYSTEMS
Immunity test IEC 60601 test level Compliance level
Electrostatic discharge
(ESD)
IEC 61000-4-2
±8 kV contact
±15 kV air ±8 kV contact
±15 kV air
Radiated RF
IEC 61000-4-3 20V/m
80MHz
～
2.7GHz
20V/m
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
30A/m 30A/m
Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless
communications equipment