ActivePure F171A Руководство - Страница 14

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ActivePure F171A Руководство

DEVICE IEC 60601-1-2:2014 EMC INFORMATION

This device passed each of the 11 tests, as indicated. Immunity test levels performed on the device,
• Electrostatic Discharge Immunity – Tested at 2,4,8 and 15 kV
• Radiated Immunity – Tested 3 V/m (Professional Healthcare) and 10 V/m (Home Healthcare)
• Conducted Immunity – Tested 150 Hz ~ 80 MHz with AM 80% @ 1kHz 3V and 6V
TEST STANDARD
Conducted Emissions (EN 55011, CISPR 11)
Radiated Emissions (EN 55011, CISPR 11)
Harmonics (EN 61000-3-2)
Flicker (EN 61000-3-3: IEC 61000-4-2)
Electrostatic Discharge (EN 61000-4-2: IEC 6100-4-2)
Radiated Immunity (EN 61000-4-3: IEC 61000-4-3)
Fast Transient Burst (EN 61000-4-4: IEC 61000-4-4)
Surges (EN 61000-4-5: IEC 61000-4-5)
Conducted Immunity (EN 61000-4-6: IEC 61000-4-6)
Power Frequency Magnetic Field (EN 61000-4-8: IEC 61000-4-8)
Voltage Dips and Interrupt (EN 61000-4-11: IEC 61000-4-11)
• This device conforms fully to the EMC requirement of IEC 60601-1-2 and is suitable for use in a professional healthcare environment
• This device is not effected by RFID, wireless networks, 2-ways radios, paging systems, etc., as the device does not transmit or receive RF signals
or create EMF beyond the required limits
• Do not use device with an extension cord as unintended EMF may be created
• This device is grounded to prevent electrostatic discharge
• Do not use RF communication or magnetic field generating equipment within 30 cm of the device
• EMC testing shows no conducted or radiated electromagnetic emissions or immunity issues which would be adverse to the patient or operator
The use of this device in a manner other than described in the user manual or a modification of the device could result in
increased electromagnetic emissions or decreased immunity.
If device is operating in an unexpected manner or causing unexpected interference, discontinue using the device, review the
user manual or seek service.
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