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8000-INS-UMENG Rev. 4
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Electromagnetic Compatibility
Like other medical equipment, the DGH 8000 Scanmate-B requires special precautions
to ensure electromagnetic compatibility with other electrical medical devices. To ensure
electromagnetic compatibility (EMC), the DGH 8000 must be installed and operated
according to the EMC information provided in this manual.
The DGH 8000 has been designed and tested to comply with EN 60601-1-2
requirements for EMC with other devices.
Guidance and Manufacturer’s Declaration: Electromagnetic Emissions
The DGH 8000 Probe is intended for use in the electromagnetic environment specified below. The customer
or the user of the USB Ultrasound Probe should ensure that it is used in such an environment.
Emissions Test
Test Level
Compliance Level
Electromagnetic Environment - Guidance
Conducted Emissions
EN 55011:2009+A1:2010,
CISPR 11:2009+A1:2010
Class A Group 1
150 kHz to 30 MHz
Complies
The device uses RF energy for its internal function.
Nearby electronic equipment may be affected.
Radiated Emissions
EN 55011:2009+A1:2010,
CISPR 11:2009+A1:2010
Class A Group 1
30 MHz to 1 GHz
Complies
Mains power quality should be that of a typical
commercial or hospital environment. If the user of the
device requires continued operation during power
mains interruptions, it is recommended that the
device be powered from an uninterruptible power
supply or battery.
Harmonics
IEC/EN 61000-3-2:2006
/A2:2014
Class A Device
Complies
Per Clause 5 of the
Standard
Flicker
IEC/EN 61000-3-3:2013
Per Clause 5 of the
Standard
Complies
Per Clause 5 of the
Standard
! CAUTION
Portable and mobile RF communications equipment may affect the normal
function of the DGH 8000 Scanmate-B.
! CAUTION
Do not use cables or accessories other than those provided with the DGH 8000
Scanmate-B, as they may result in increased electromagnetic emissions or
decrease immunity to such emissions.
