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Electromagnetic Compatibility
Like other electrical medical equipment, the L9000 requires special precautions to
ensure electromagnetic compatibility with other electrical medical devices. To
ensure electromagnetic compatibility (EMC), the L9000 must be installed and
operated according to the EMC information provided in this manual.
Note The L9000 has been designed and tested to comply with IEC
60601-1-2:2001 requirements for EMC with other devices.
Caution Equipment which employs radio frequency (RF)
communications may affect the normal function of the L9000.
W
ARNING DO NOT USE CABLES OR ACCESSORIES OTHER THAN THOSE
PROVIDED WITH THE L9000, AS THIS MAY RESULT IN INCREASED
ELECTROMAGNETIC EMISSIONS OR DECREASED IMMUNITY TO
SUCH EMISSIONS.
W
ARNING IF THE L9000 IS USED ADJACENT TO OR STACKED WITH OTHER
EQUIPMENT, OBSERVE AND VERIFY NORMAL OPERATION OF THE
L9000
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 L9000.
Guidance and Manufacturer's Declaration: Electromagnetic Emissions
L9000 is intended for use in the electromagnetic environment specified below. The customer or the
user of L9000 should ensure that it is used in such an environment.
Emissions test Compliance Electromagnetic Environment - guidance
RF emissions CISPR
11
Class B
L9000 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
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