Introduction
5
Product Compliance:
Emission & Immunity Standards
The ForeSite SS is a class A digital device suitable for business, industrial and
commercial environments. It is not intended for residential use. The ForeSite
SS may cause radio interference or may disrupt the operation of nearby
equipment. Portable and mobile RF communications equipment can also
affect ForeSite SS. It may be necessary to take mitigation measures, such as
reorienting or relocating the equipment or shielding the location.
The ForeSite SS should not be used adjacent to or stacked with other
equipment. If adjacent or stacked operation is necessary, the Pressure
Imaging System should be observed to verify normal operation in the
configuration in which it will be used.
Use of accessories and cables other than those provided by XSENSOR may
result in increased emissions or decreased immunity.
ForeSite SS complies with Part 15 of the FCC Rules. Operation is subject to the
following conditions: (1) This device may not cause harmful interference, and
(2) This device must accept any interference received, including interference
that may cause undesired operation.
Standards Compliance:
√
EN 60601-1-2:2007 (Ed3.0) Medical Electrical Equipment – Part 1:
General Requirements for Safety 2. Collateral Standard: Electromagnetic
Compatibility (Non-life-supporting, Group 1, Class A Equipment)
√
FCC 15.107/CISPR 11 (Class A) Conducted Emissions
√
FCC 15.109/CISPR 11 (Class A) Radiated Emissions
√
Industry Canada ICES-003(A)/NMB-3(A) Compliant
√
IEC 61000-3-2:2005 Harmonics Emissions
√
IEC 61000-3-3:2008 Flicker Emissions
√
IEC 61000-4-2:2008 Electrostatic Discharge
√
IEC 61000-4-3:2008 Radiated Susceptibility
√
IEC 61000-4-4:2007 Electrical Fast Transients
√
IEC 61000-4-5:2005 Surge Susceptibility
√
IEC 61000-4-6:2006 Conducted Susceptibility
√
IEC 61000-4-8:2001 Magnetic Susceptibility
√
IEC 61000-4-11:2007 Dips & Interrupts
Содержание ForeSite SS
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