Electromagnetic Compatibility Information - Beurer FM 150 Mode D'emploi

Electromagnetic Compatibility Information

This product can only use speciied power supply and components. If diferent power supply or component is
used, then the electromagnetic emission and immunity to interference of the product might be afected.
Under normal working environment and the existence of other equipments, the product can work normally, but
its therapeutic function may be afected. In order to avoid being disturbed by other equipments, we suggest that
you pay attention to the following matters while using the product:
• under room temperature
• please connect to 100-240 VAC power supply or use 4 AA (LR6) dry batteries
• avoid placing the product near electromagnetic ield (such as mobile phone, microwave oven).
Table 1
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture's declaration – electromagnetic emission
The device is intended to be used in the following speciied electromagnetic environment, buyer or user should make sure
that it's being used in such electromagnetic environment.
Emissions test
RF emissions CISPR 11
RF emissions CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage luctuations/
licker emissions IEC 61000-3-3
Table 2
Guidance and manufacturer's declaration – electromagnetic immunity
The device is intended to be used in the following speciied electromagnetic environment, buyer or user of the device
should make sure that it's being used in such electromagnetic environment.
Immunity test
Electrostatic discharge
(ESD) IEC 61000-4-2
Electrical fast transient/
burst IEC 61000-4-4
Surge IEC 61000-4-5
Voltage dips, short
interruptions and vol-
tage variations on
power supply input lines
IEC 61000-4-11
Power frequency
(50Hz/60Hz) magnetic
ield IEC 61000-4-8
NOTE: U is the a.c. mains voltage prior to application of the test level.
T
Compliance Electromagnetic environment – Manual
Group 1 The device only uses RF energy for its internal functions, so its RF emis-
sion is relatively low which may not cause any interference to electronic
equipments nearby.
Class B The device is suitable to be used in all facilities, including household and
public low-voltage power supply network which is directly connected to
Class A
residence for domestic use.
Complies
IEC 60601 test level
±6 kV contact
±8 kV air
Electrical fast transient/
burst IEC 61000-4-4
± 1kV line(s) and neutral ± 1kV line(s) and neutra
<5 % U
T
(>95 % dip in U )
T
for 0.5 cycle
40 % U
T
(60 % dip in U )
T
for 5 cycles
70 % U
T
(30 % dip in U )
T
for 25 cycles
<5 % U
T
(>95 % dip in U )
T
for 5 s
3 A/m
Compliance level
±6 kV contact
±8 kV air
±2kV for power supply
lines
<5 % U
T
(>95 % dip in U )
T
for 0.5 cycle
0 % U
T
(60 % dip in U )
T
for 5 cycles
70 % U
T
(30 % dip in U )
T
for 25 cycles
5 % U
T
(>95 % dip in U )
T
for 5 s
3 A/m
85
Electromagnetic environment – guidance
Floors should be wood, concrete or cera-
mic tile. If loors are covered with synthetic
material, the relative humidity should be at
least 30%.
Mains power quality should be that of a typi-
cal commercial or hospital environment.
Mains power quality should be that of a typi-
cal commercial or hospital environment.
Mains power quality should be that of a typi-
cal commercial or hospital environment. If
the user of the Neck Electronic Muscle Sti-
mulator requires continued operation during
power mains interruptions, it is recommen-
ded that the Neck Electronic Muscle Sti-
mulator be powered from an uninterruptible
power supply or a battery.
Power frequency magnetic ields should be
at levels characteristic of a typical location
in a typical commercial or hospital environ-
ment.