ActivePure F170A Manuel - Sayfa 14

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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.