SOPRO COMEG SYMBIOZ Flow Manual De Usuario página 31

12
12-2 Manufacturer's guide and declaration – electromagnetic immunity
This insufflator was designed to be used in the electromagnetic environment specified below. The user must ensure that it is in fact
used in this environment.
safety test ieC 60601
level of gravity
electrostatic discharges ± 6 kV via Contact
en 61000-4-2 ± 8 kV via l'air
Rapid transient peaks ± 2 kV electric lines
en 61000-4-4 ± 1 kV input/output
lines
electric shocks Differential mode
en 61000-4-5 ± 1 kV
shared mode
± 2 kV
Power failures, short • <5% UT –
power interruptions and 10 ms
variations in voltage • 40% UT –
en 61000-4-11 100 ms
• 70% UT –
500 ms
• <5% UT –
5 s
system frequency 3 A/m
magnetic field (50/60
hz) ieC61000-4-8
note: UT is the nominal value of the electrical voltage applied during the test.
eleCTROMAgneTiC COMPATiBiliTY
Compliance
level
± 6 kV
± 8 kV
± 2 kV
± 1 kV
± 1 kV
± 2 kV
<5% UT
10 ms
<40% UT
100 ms
<70% UT
500 ms
<5% UT
5 s
3 A/m
electromagnetic environment - guide
The floor must be wooden, concrete or tiled. if the floor is covered
with synthetic material, the relative humidity must be at least 30%.
The quality of the electric power supply must be that of a commer-
cial or typical hospital environment.
The quality of the electric power supply must be that of a commer-
cial or typical hospital environment.
The quality of the electric power supply must be that of a commer-
cial or typical hospital environment.
if the user of this insufflator must be able to continue working
during power interruptions, it is advisable for this insufflator to be
supplied with power from a UPs or battery.
The system frequency magnetic field must be at a level that is
characteristic of a his (health information system) location (50 /
60 hz) in a commercial or typical hospital environment.
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