Philips Azurion - 16.22 Electromagnetic Compatibility

Figure 145 Dose pr
ole for an XperCT acquision with a detector eld size of 48 cm
Legend
1 Normalized scale (%)
2 Distance from the isocenter along the Z-axis (mm)
16.22 Electr
omagnec Compability
You should only use the system in an electromagnec environment similar to the environment
described in this secon.
WARNING
Do not ac
quire X-ray images while acvely using electrosurgical devices (for example, electrosurgical
knives), or cardiac debrillators. The electromagnec interference generated by these devices may
reduce image quality, resulng in addional exposure runs being required.
WARNING
The use of ac
cessories, transducers, and cables other than those specied for this equipment may
result in increased emissions or decreased immunity.
WARNING
The equipmen
t should not be used adjacent to, or stacked with, other equipment. If adjacent or
stacked use is necessary, the operator must verify that the system operates normally in the
conguraon in which it will be used.
Electromagnec Emissions
The following table provides the manufacturer's declaraon and guidance concerning electromagnec
emissions.
Emission test Compliance Guidance
Radiated RF emissions
CISPR 11
Group 1 Class A The system uses RF energy only for their internal funcons.
Ther
efore, its RF emissions are low and not likely to cause
any interference in nearby electronic equipment.
Technical In
formaon Electromagnec Compability
Azurion Release 1.2 Ins
trucons for Use 322 Philips Healthcare 4522 203 52421