This document specifies test methodologies for the evaluation of the electromagnetic compatibility (EMC) of active implantable cardiovascular devices that provide one or more therapies for bradycardia, tachycardia and cardiac resynchronization in conjunction with transvenous lead systems.

NOTE This document was designed for pulse generators used with endocardial leads or epicardial leads. At the time of this edition, the authors recognized the emergence of technologies that do not use endocardial leads or epicardial leads for which adaptations of this part will be required. Such adaptations are left to the discretion of manufacturers incorporating these technologies.

Cross References:
ISO 14708-1:2014
BS EN ISO 14708-2:2019
ISO 14708-6:2019
ISO 14708-2:2019
BS EN ISO 14708-6:2019
EN 301489-35
EN 50527-1
ISO/IEC Guide 51
IEEE C95.1:2005
EN 45502-2-2
EN 50527-2-1
ERC Recommendation 70-03
IEEE Std 802.15.6-2012
DIN VDE 0848-3-1
EN 301489-1
ANSI/AAMI PC69:2000
EN 301489-27
IEEE C95.6:2003
EN 50061
EN 45502-2-1
ANSI/AAMI PC69:2007
ANSI C63.5-1988
prEN 50527-2-2
EN 301489-29
EN 301489-31
ISO 11318:2002
ISO 5841-3:2013
ISO 27186:2010


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