GE Corometrics 170 Series Service Manual
Electromagnetic compatibility (emc) and electrostatic discharge (esd)
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Also See for Corometrics 170 Series:
- Operator's manual (112 pages) ,
- Service manual (248 pages)
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Addendum to Corometrics® 170 Series Service Manual
Electromagnetic Compatibility (EMC) and
Electromagnetic Compatibility (EMC)
Corometrics Model 171
Revision A
September, 2004
Changes or modifications to this system not expressly approved by
GE Medical Systems can cause EMC issues with this or other
equipment. This system is designed and tested to comply with
applicable regulation regarding EMC and must 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.
Corometrics® 170 Series
2000947-007
PN 2000947-007
1
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Table of Contents
Related Manuals for GE Corometrics 170 Series
Summary of Contents for GE Corometrics 170 Series
- Page 1 Corometrics Model 171 Changes or modifications to this system not expressly approved by GE Medical Systems can cause EMC issues with this or other equipment. This system is designed and tested to comply with applicable regulation regarding EMC and must be installed and put into service according to the EMC information stated as follows.
- Page 2 Guidance and Manufacturer’s Declaration – Electromagnetic Emissions The Corometrics Antepartum Monitor, Model 171, is intended for use in the electromagnetic environment specified below. It is the responsibility of the customer or user to assure that the Corometrics Antepartum Monitor, Model 171, is used in such an environment. Emissions Test Compliance Electromagnetic Environment –...
- Page 3 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The Corometrics Antepartum Monitor, Model 171 is intended for use in the electromagnetic environment specified below. It is the responsibility of the customer or user to assure that the Corometrics Antepartum Monitor, Model 171 is used in such an environment. Immunity Test EN 60601 Test Level Compliance Level...
- Page 4 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The Corometrics Antepartum Monitor, Model 171, is intended for use in the electromagnetic environment specified below. It is the responsibility of the customer or user to assure that the Corometrics Antepartum Monitor, Model 171, is used in such an environment. Immunity Test EN 60601 Test Level Compliance Level...
- Page 5 Recommended Separation Distances The table below provides the recommended separation distances (in meters) between portable and mobile RF communication equipment and the Corometrics Antepartum Monitor, Model 171.The Corometrics Antepartum Monitor, Model 171, is intended for use in the electromagnetic environment on which radiated RF disturbances are controlled.
- Page 6 The table below lists cables, transducers, and other applicable accessories with which GE Medical Systems claims EMC compliance. NOTE: Any supplied accessories that do not affect EMC compliance are not included. Part No...
- Page 7 Corometrics Model 172 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.
- Page 8 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The Corometrics Antepartum Monitor, Model 172 is intended for use in the electromagnetic environment specified below. It is the responsibility of the customer or user to assure that the Corometrics Antepartum Monitor, Model 172 is used in such an environment. Immunity Test EN 60601 Test Level Compliance Level...
- Page 9 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The Corometrics Antepartum Monitor, Model 172, is intended for use in the electromagnetic environment specified below. It is the responsibility of the customer or user to assure that the Corometrics Antepartum Monitor, Model 172, is used in such an environment. Immunity Test EN 60601 Test Level Compliance Level...
- Page 10 Recommended Separation Distances The table below provides the recommended separation distances (in meters) between portable and mobile RF communication equipment and the Corometrics Antepartum Monitor, Model 172.The Corometrics Antepartum Monitor, Model 172, is intended for use in the electromagnetic environment on which radiated RF disturbances are controlled.
- Page 11 The table below lists cables, transducers, and other applicable accessories with which GE Medical Systems claims EMC compliance. NOTE: Any supplied accessories that do not affect EMC compliance are not included. Part No...
- Page 12 Corometrics Model 173 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.
- Page 13 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity 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. Immunity Test EN 60601 Test Level Compliance Level...
- Page 14 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity 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. Immunity Test EN 60601 Test Level Compliance Level...
- Page 15 Recommended Separation Distances The table below provides the recommended separation distances (in meters) between portable and mobile RF communication equipment and the Corometrics Intrapartum Monitor, Model 173. The Corometrics Intrapartum Monitor, Model 173, is intended for use in the electromagnetic environment on which radiated RF disturbances are controlled.
- Page 16 The table below lists cables, transducers, and other applicable accessories with which GE Medical Systems claims EMC compliance. NOTE: Any supplied accessories that do not affect EMC compliance are not included. Part No...
- Page 17 Part No Description Maximum Lengths Telemetry Cable 1563AAO 120/340 Interface Cable 3m / 10ft Accessories 2020760-001 NeST AC/DC Power Supply 600028 AC cord, Hospital grade, AHA 2.4m / 8ft 600034 AC cord, Hospital grade, IEC 2.4m / 8ft 600049 AC cord, Hospital grade, UK 2.4m / 8ft Revision A Corometrics®...
- Page 18 Corometrics Model 174 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.
- Page 19 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The Corometrics Intrapartum Monitor, Model 174, 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 174, is used in such an environment. Immunity Test EN 60601 Test Level Compliance Level...
- Page 20 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The Corometrics Intrapartum Monitor, Model 174, 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 174, is used in such an environment. Immunity Test EN 60601 Test Level Compliance Level...
- Page 21 Recommended Separation Distances The table below provides the recommended separation distances (in meters) between portable and mobile RF communication equipment and the Corometrics Intrapartum Monitor, Model 174. The Corometrics Intrapartum Monitor, Model 174, is intended for use in the electromagnetic environment on which radiated RF disturbances are controlled.
- Page 22 The table below lists cables, transducers, and other applicable accessories with which GE Medical Systems claims EMC compliance. NOTE: Any supplied accessories that do not affect EMC compliance are not included. Part No...
- Page 23 Part No Description Maximum Lengths Accessories 2020760-001 NeST AC/DC Power Supply 600028 AC cord, Hospital grade, AHA 2.4m / 8ft 600034 AC cord, Hospital grade, IEC 2.4m / 8ft 600049 AC cord, Hospital grade, UK 2.4m / 8ft Revision A Corometrics®...
- Page 24 Corometrics Model 173 and Model 174 monitors. Following is an updated list of symbols used on products manufactured by GE. This table appears in Chapter 1, page 1-7, of your Operator Manual. Some symbols may not appear on your unit.
- Page 25 Placement of ESD Symbol on Monitor Revision History Each page of the document has the document part number and revision letter at the bottom of the page. The revision letter changes each time the document is updated. Revision Date Comment September 14, 2004 Initial Release Revision A...
- Page 26 GE Medical Systems Information Technologies 8200 W. Tower Ave., Milwaukee, WI 53223 U.S.A. © 2004 GE Medical Systems Information Technologies. All rights reserved. 0459 World Headquarters European Representative Asia Headquarters GE Medical Systems GE Medical Systems GE Medical Systems Information Technologies, Inc.