Electromagnetic Conformity - Hikoneb 908 DC Benutzerhandbuch

H i k o n e b | 9 0 8 D C
Us e r Ma n ua l
Nebulization Chamber
Weight
Internal Volume
Operation Volume

13. Electromagnetic Conformity

The nebulizer can operate without being affected by electromagnetic frequencies at a
certain level. Ultrasonic Nebulizers Electromagnetic Conformity Directive (89/336/AT).
The device has been tested and manufactured conforming to the Medical Devices
EEC/93/42 Medical Devices Rules and EN 60601-1 and EN60601-1-2 Electromagnetic
conformity. EMC Test.
Test
TS EN 61000-4-2
Electrostatic Discharge
Immunity
TS EN 61000-4-3
Beaming, RF, Electro
Magnetic Area Immunity
TS EN 61000-4-4
Electrical Rapid Temporary
Regime/ Explosion
İmmunity
TS EN 61000-4-5
Immunity Against Sudden
Increases
TS EN 61000-4-6
Its Immunity Against
Inducted and Transmitted
Breaks by RF Areas
22
Level
With contact: ± 8 kV
From air: ± 2 – 4 – 8 -
15 kV
10V
±2 kV 100 kHz
L-N: ± 0,5 - 1 - 2 kV
L-PE: ± 0,5 - 1 - 2 kV
3 V
0.407kg
0.743L
0.277 – 0.348L
Ambient
Laying where the device is placed,
should be wooden, concrete or
ceramic. If laying is synthetic, relative
humidity should be 30% at least.
Portable and movable RF devices
should not be approached to our
device. Required distances have been
given below.
Power feeding should be on mains or
hospital installation quality, in building
power input, Leakage Current Protective
Relay should be plugged if there is not.
Power feeding should be on mains or
hospital installation quality, in building
power input, Leakage Current Protective
Relay should be plugged if there is not.
Portable and movable RF devices
should not be approached to our
device. Required distances have been
given below.