BS EN ISO 11073-10103:2013

Foreword
1 Overview
2 Normative references
3 Definitions, acronyms, and abbreviations
4 Introduction to IEEE 11073 implantable
  devices cardiac domain
5 Nomenclature requirements
6 Nomenclature structure
7 Conformance
8 Extensibility/versioning
Annex A (normative) - Base terms
Annex B (informative) - Base terms additional
         properties
Annex C (normative) - Expanded terms with
         Systematic name and codes
Annex D (normative) - Enumerations
Annex E (informative) - Vendor enumerations
Annex F (informative) - Example report
Annex G (informative) - Implementation notes
Annex H (informative) - Schema and XML for
         nomenclature
Annex I (informative) - Bibliography
Annex J (informative) - IEEE list of participants

Describes the base nomenclature provided in ISO/IEEE 11073-10101:20041 to support terminology for implantable cardiac devices.

This standard extends the base nomenclature provided in ISO/IEEE11073-10101:2004¹ to support terminology for implantable cardiac devices. Devices within the scope of this nomenclature are implantable devices such as pacemakers, defibrillators, devices for cardiac resynchronization therapy, and implantable cardiac monitors. This nomenclature defines the discrete terms necessary to convey a clinically relevant summary of the information obtained during a device interrogation. The nomenclature extensions may be used in conjunction with other IEEE 11073 standard components (e.g., ISO/IEEE11073-10201 [B2]²) or with other standards, such as Health Level Seven International (HL7).