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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.
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