Electromagnetic Compatibility Tables
27
Like other electrical medical equipment, the X7000 requires special
precautions to ensure electromagnetic compatibility with other electrical
medical devices. To ensure electromagnetic compatibility (EMC), the
X7000 must be installed and operated according to the EMC information
provided in this manual.
Note
The X7000 has been designed and tested to comply with
IEC 60601-1-2:2001 requirements for EMC with other
devices.
Caution
Portable and mobile RF communications equipment may
affect the normal function of the X7000.
Warning Do not use cables or accessories other than those
provided with the X7000, as this may result in
increased electromagnetic emissions or decreased
immunity to such emissions.
Warning
If the X7000 is used adjacent to or stacked with other
equipment, observe and verify normal operation of the
X7000 in the configuration in which it will be used prior
to using it in a surgical procedure. Consult the tables
below for guidance in placing the X7000.
Guidance and Manufacturer's Declaration: Electromagnetic Emissions
X7000 is intended for use in the electromagnetic environment specified below. The customer or the
user of X7000 should ensure that it is used in such an environment.
Emissions test
Compliance
Electromagnetic Environment - guidance
RF emissions CISPR
11
Group 1
X7000 uses RF energy only for its internal
function; therefore, its RF emissions are very
low and are not likely to cause any interference
in nearby electronic equipment.
RF emissions CISPR
11
Class B
X7000 is suitable for use in all establishments,
including domestic establishments and those
directly connected to the public low-voltage
power supply network that supplies buildings
used for domestic purposes.
Harmonic emissions
IEC61000-3-2
Class A
Voltage Fluctuations/
flicker emissions
IEC61000-3-3
Complies
Electromagnetic Compatibility
Summary of Contents for X7000
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