Hikoneb 908 DC, Руководство пользователя

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H i k o n e b | 9 0 8 D C
22
User Manual
Weight 0.407kg
Internal Volume 0.743L
Operation Volume 0.277 – 0.348L
Nebulization Chamber
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 Level Ambient
TS EN 61000-4-2
Electrostatic Discharge
Immunity
With contact: ± 8 kV
From air: ± 2 – 4 – 8 -
15 kV
Laying where the device is placed,
should be wooden, concrete or
ceramic. If laying is synthetic, relative
humidity should be 30% at least.
TS EN 61000-4-3
Beaming, RF, Electro
Magnetic Area Immunity
10V
Portable and movable RF devices
should not be approached to our
device. Required distances have been
given below.
TS EN 61000-4-4
Electrical Rapid Temporary
Regime/ Explosion
İmmunity
±2 kV 100 kHz
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.
TS EN 61000-4-5
Immunity Against Sudden
Increases
L-N: ± 0,5 - 1 - 2 kV
L-PE: ± 0,5 - 1 - 2 kV
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.
TS EN 61000-4-6
Its Immunity Against
Inducted and Transmitted
Breaks by RF Areas
3 V
Portable and movable RF devices
should not be approached to our
device. Required distances have been
given below.