IEEE/ANSI C63.18-2014
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
American National Standard Recommended Practice for an On-Site, Ad Hoc Test Method for Estimating Electromagnetic Immunity of Medical Devices to Radiated Radio-Frequency (RF) Emissions from RF Transmitters
Hardcopy , PDF
31-10-2024
English
20-06-2014
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1 Overview
2 Caveats and limitations
3 Overview of the test
4 Preparation for testing
5 Testing
6 Use of the test results in determining
minimum separation distances
7 Test report
8 Correlation of test results to laboratory
immunity testing
9 Use of test results in EMI policies and
procedures
Annex A (informative) - EMC standards and
guidelines containing radiated RF
immunity requirements that are or
could be applicable to medical devices
Annex B (informative) - Characteristics and
types of RF transmitters
Annex C (informative) - Alternative RF test
sources and test methods
Annex D (informative) - Estimation of incident
field strength and minimum test distance
without the use of an E-field meter
Annex E (informative) - Obtaining appropriate
experimental licenses
Annex F (informative) - Recommendations for
mitigation of EMI in health-care facilities
Annex G (informative) - Sample test data sheets
Annex H (informative) - Bibliography
This recommended practice is a guide to evaluating the electromagnetic immunity of medical devices to radiated radio-frequency (RF) emissions from common RF transmitters (e.g., two-way radios; walkie-talkies; mobile phones; wireless-enabled tablets, e-readers, laptop computers, and similar devices; radio-frequency identification (RFID) readers; networked mp3 players; two-way pagers; and wireless personal digital assistants [PDAs]).
| DocumentType |
Standard
|
| ISBN |
978-0-7381-9160-7
|
| Pages |
126
|
| PublisherName |
Institute of Electrical & Electronics Engineers
|
| Status |
Withdrawn
|
| Supersedes |
| BS EN 61326-2-6:2013 | Electrical equipment for measurement, control and laboratory use. EMC requirements Particular requirements. In vitro diagnostic (IVD) medical equipment |
| CEI EN 61326-2-6 : 2014 | ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL AND LABORATORY USE - EMC REQUIREMENTS - PART 2-6: PARTICULAR REQUIREMENTS - IN VITRO DIAGNOSTIC (IVD) MEDICAL EQUIPMENT |
| AAMI/IEC TIR80001-2-3:2012 | APPLICATION OF RISK MANAGEMENT FOR IT-NETWORKS INCORPORATING MEDICAL DEVICES - PART 2-3: GUIDANCE FOR WIRELESS NETWORKS |
| ISO/TR 21730:2007 | Health informatics Use of mobile wireless communication and computing technology in healthcare facilities Recommendations for electromagnetic compatibility (management of unintentional electromagnetic interference) with medical devices |
| PD ISO/TR 21730:2007 | Health informatics. Use of mobile wireless communication and computing technology in healthcare facilities. Recommendations for electromagnetic compatibility (management of unintentional electromagnetic interference) with medical devices |
| AAMI TIR18:2010 | GUIDANCE ON ELECTROMAGNETIC COMPATIBILITY OF MEDICAL DEVICES IN HEALTHCARE FACILITIES |
| I.S. EN 61326-2-6:2013 | ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL AND LABORATORY USE - EMC REQUIREMENTS - PART 2-6: PARTICULAR REQUIREMENTS - IN VITRO DIAGNOSTIC (IVD) MEDICAL EQUIPMENT (IEC 61326-2-6:2012 (EQV)) |
| 10/30216029 DC : 0 | BS EN 61326-2-6 - ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL AND LABORATORY USE - EMC REQUIREMENTS - PART 2-6: PARTICULAR REQUIREMENTS - IN VITRO DIAGNOSTIC (IVD) MEDICAL EQUIPMENT |
| IEC 61326-2-6:2012 | Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment |
| IEEE/ANSI C63.15-2010 | American National Standard Recommended Practice for the Immunity Measurement of Electrical and Electronic Equipment |
| PD IEC/TR 80001-2-3:2012 | Application of risk management for IT-networks incorporating medical devices Guidance for wireless networks |
| IEEE DRAFT 1073.0.1 : D01J 2006 | HEALTH INFORMATICS - POINT-OF-CARE MEDICAL DEVICE COMMUNICATION - TECHNICAL REPORT - GUIDELINES FOR THE USE OF RF WIRELESS TECHNOLOGY |
| EN 61326-2-6:2013 | Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment |
| CSA Z32 : 2015 | ELECTRICAL SAFETY AND ESSENTIAL ELECTRICAL SYSTEMS IN HEALTH CARE FACILITIES |
| IEC TR 80001-2-3:2012 | Application of risk management for IT-networks incorporating medical devices - Part 2-3: Guidance for wireless networks |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| IEEE/ANSI C63.9-2008 | American National Standard for RF Immunity of Audio Office Equipment to General Use Transmitting Devices with Transmitter Power Levels up to 8 Watts |
| IEC TR 61000-5-2:1997 | Electromagnetic compatibility (EMC) - Part 5: Installation and mitigation guidelines - Section 2: Earthing and cabling |
| ISO/TR 21730:2007 | Health informatics Use of mobile wireless communication and computing technology in healthcare facilities Recommendations for electromagnetic compatibility (management of unintentional electromagnetic interference) with medical devices |
| IEC 60601-1-2:2014 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
| AAMI TIR18:2010 | GUIDANCE ON ELECTROMAGNETIC COMPATIBILITY OF MEDICAL DEVICES IN HEALTHCARE FACILITIES |
| IEEE/ANSI C63.12-2015 | American National Standard Recommended Practice for Electromagnetic Compatibility Limits and Test Levels |
| IEC 61000-4-3:2006+AMD1:2007+AMD2:2010 CSV | Electromagnetic compatibility (EMC) - Part 4-3: Testing and measurement techniques - Radiated, radio-frequency, electromagnetic field immunity test |
| IEC TR 61000-5-6:2002 | Electromagnetic compatibility (EMC) - Part 5-6: Installation and mitigation guidelines - Mitigation of external EM influences |
| IEC 61000-6-1:2016 | Electromagnetic compatibility (EMC) - Part 6-1: Generic standards - Immunity standard for residential, commercial and light-industrial environments |
| IEC TR 61000-5-1:1996 | Electromagnetic compatibility (EMC) - Part 5: Installation and mitigation guidelines - Section 1: General considerations - Basic EMC publication |
| RTCA DO 294 : C2008 | GUIDANCE ON ALLOWING TRANSMITTING PORTABLE ELECTRONIC DEVICES (T-PEDS) ON AIRCRAFT |
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