Photonic PL Serie Manual De Operación página 6

EMC WARNINGS
This chapter describes the measures required in EN60601-1-2 (electromagnetic
compatibility) for ensuring electromagnetic compatibility (EMC).
Medical electrical equipment are subject to special precautionary mea-
sures with respect to EMC. Failure to observe these instructions can
lead to an increased emission or a reduced noise immunity of the device or sys-
tem! Portable and mobile HF communications equipment can affect medical
electrical equipment!
In the medical area and application, use only accessories designated for
this purpose by the manufacturer!
Electromagnetic emission
This device is intended for use in the electromagnetic environment specified below.
The customer or the user of this device should assure that it is used in such an environment.
Emission test
RF-emissions
CISPR 11
RF-emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/flicker emissions
IEC 61000-3-3
RF-emissions
CISPR 15
Electromagnetic immunity
This device is intended for use in the electromagnetic environment specified below.
The customer or the user of this device should assure that it is used in such an environment.
Immunity test
Electrostatic discharge
IEC 61000-4-2
Electrical fast transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short interruptions
and voltage variations on power supply input lines
IEC 61000-4-11
Power frequency (50 Hz/60 Hz)
magnetic field
IEC 61000-4-8
NOTE: U is the a.c. mains voltage prior to application of the test level.
T
Overens-stemmelse Electromagnetic environment – guidance
Group 1 This device 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.
Class B This device is suitable for use in all establishments, including domestic establishments and those
directly connected to the public low-voltage power supply network that supplies buildings used for
domestic purposes.
Class C
Complies
Complies
IEC 60601 test level and Compliance level
± 6 kV contact
± 8 kV air
± 2 kV for power supply lines
± 1 kV for input/output lines (not applicable)
± 1 kV differential mode
± 2 kV common mode
< 5 % U (> 95 % dip in U ) for 1/2 cycle
T T
40 % U (60 % dip in U ) for 5 cycles
T T
70 % U (30 % dip in U ) for 25 cycles
T T
< 5 % U (> 95 % dip in U ) for 5 s
T T
3 A/m
Do not place the device immediately next to other devices and avoid stacking
with other devices. However, if doing so cannot be avoided, device and system
must be closely monitored so that normal operation in this arrangement can be
checked!
Use only the supplied power cables (max. length 2.5 m)! Longer and different
power cables can lead to an increased emission or a reduced noise immunity of
the device or system!
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 %.
Mains power quality should be that of a typical commercial or hospi-
tal environment.
Mains power quality should be that of a typical commercial or hospi-
tal environment.
Mains power quality should be that of a typical commercial or hospi-
tal environment. If the use of this device requires continued operation
during power mains interrupts, it is recommended that this device be
powered from an uninterruptible power supply or a battery.
Power frequency magnetic fields should be at levels characteristic of
a typical location in a typical commercial or hospital environment.