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Manufacturer’s declaration and guide – electromagnetic emissions
The medical bed (see references in contents) has been designed for use in the electromagnetic environment specified below. The user should ensure that it is used in such
an environment.
Emissions test
Compliance
Electromagnetic environment - Guide
RF emissions
CISPR 11
Group 1
The medical bed (see references in contents) uses RF energy only for its internal functions.
Therefore, its RF emissions are very low and are not likely to cause any interference in nearby
electronic equipment.
RF emissions
CISPR 11
Class B
Harmonic emissions
EN 61000-3-2
Class A
Voltage fluctuations / Flicker
EN 61000-3-3
Applicable
The medical bed (see references in contents) can be used in all domestic environments,
including those directly connected to the public low-voltage power supply network that supplies
buildings for domestic purpose.
[ ]
RF emissions
CISPR 14-1
Compliant
The medical bed (see references in contents) has not been designed for connection to other
equipment.
Manufacturer’s declaration and guide - electromagnetic immunity
The medical bed (see references in contents) has been designed for use in the electromagnetic environment specified below. The user should ensure that it is used in such
an environment.
Immunity test
IEC 60601
Severity level
Compliance level
Electromagnetic environment - Guide L
Electrostatic discharge
EN 61000-4-2
±
6 kV contact
±
8 kV air
±
6 kV contact
±
8 kV air
Floors should be wood, concrete, or ceramic tile. If floors are covered with
synthetic material, the relative humidity should be at least 30%.
Electrical fast transients
EN 61000-4-4
±
2 kV for feeders
±
1 kV for input/output lines
±
2 kV for feeders
±
1 kV for input/output lines
The quality of the main power supply must be the same as for a typical
commercial or hospital environment.
Surges
EN 61000-4-5
Differential mode
±
1 kV
Common mode
±
2 kV
Differential mode
±
1 kV
/
The quality of the main power supply must be the same as for a typical
commercial or hospital environment.
Voltage dips, short
interruptions and voltage
variations
EN 61000-4-11
•
<5% U
T
- for 10 ms
•
40% U
T
- for 100 ms
•
70% U
T
- for 500 ms
•
<5% U
T
- for 5 s
•
<5% U
T
– for 10 ms
•
40% U
T
- for 100 ms
•
70% U
T
- for 500 ms
•
<5% U
T
- for 5 s
The quality of the main power supply must be the same as for a typical
commercial or hospital environment.
If the user of the medical bed (see references in contents) wants to be
able to continue to use the bed during interruptions in the main power
supply, it is recommended that the bed be powered by a converter or
battery.
Power frequency
magnetic field
(50/60 Hz)
3 A/m
3 A/m
Power frequency magnetic fields should be at levels characteristic of a
location in a typical commercial or hospital environment.
NB: U
T
is the nominal value of power voltage applied during the test.
Manufacturer’s declaration and guide - electromagnetic immunity
The medical bed (see references in contents) has been designed for use in the electromagnetic environment specified below. The user should ensure that it is used in such
an environment.
Immunity test
IEC 60601
Severity level
Compliance level
Electromagnetic environment - Guide
Portable and mobile RF communications equipment should be used no closer to the medical
bed (see references in contents), including leads, than the recommended separation
distance, calculated using equations applicable to the frequency of the transmitter.
Recommended separation distance
Conducted RF
EN 61000-4-6
3 Vrms
150 kHz to 80 MHz
3 V
P
d
17
,
1
=
Radiated RF
EN 61000-4-3
3 V/m
80 MHz to 2.5 GHz
3 V/m
80 to 800 MHz
P
d
17
,
1
=
80 MHz to 800 MHz
P
d
33
,
2
=
800 MHz to 2.5 GHz
2 to 2.5 GHz
10 V/m
where
P
is the maximum output power rating of the transmitter in watts (W) according to