Corometrics Model 173 - GE Corometrics 170 Series Service Manual

Corometrics Model 173

Guidance and Manufacturer's Declaration - Electromagnetic
Emissions
Emissions Test
RF Emissions
EN 55011
RF Emissions
EN 55011
Harmonic Emissions
EN 61000-3-2
Voltage Fluctuations/
Flicker Emissions
EN 61000-3-3
12
Changes or modification to this system not expressly approved by GE
Medical Systems could cause EMC issues with this or other
equipment. This system is designed and tested to comply with
applicable regulation regarding EMC and needs to be installed and
put into service according to the EMC information stated as follows.
WARNING
Use of portable phones or other radio frequency (RF) emitting
equipment near the system may cause unexpected or adverse
operation.
WARNING
The equipment or system should not be used adjacent to, or
stacked with, other equipment. If adjacent or stacked use is
necessary, the equipment or system should be tested to verify
normal operation in the configuration in which it is being
used.
The Corometrics Intrapartum Monitor, Model 173, is intended for
use in the electromagnetic environment specified below. It is the
responsibility of the customer or user to assure that the Corometrics
Intrapartum Monitor, Model 173, is used in such an environment.
Compliance
Group 1 The equipment 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.
Class B
Not applicable The equipment 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.
Not applicable
Corometrics® 170 Series
2000947-007
Electromagnetic Environment – Guidance
Revision A