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>UNE standards>UNE EN ISO/IEEE 11073-10103:2025 - Health informatics - Device interoperability - Part 10103: Nomenclature, implantable device, cardiac (ISO/IEEE 11073-10103:2025) (Endorsed by Asociación Española de Normalización in November of 2025.)
in stockReleased: 2025-11-01
UNE EN ISO/IEEE 11073-10103:2025 - Health informatics - Device interoperability - Part 10103: Nomenclature, implantable device, cardiac (ISO/IEEE 11073-10103:2025) (Endorsed by Asociación Española de Normalización in November of 2025.)

UNE EN ISO/IEEE 11073-10103:2025

Health informatics - Device interoperability - Part 10103: Nomenclature, implantable device, cardiac (ISO/IEEE 11073-10103:2025) (Endorsed by Asociación Española de Normalización in November of 2025.)

Informática sanitaria. Interoperabilidad de dispositivo. Parte 10103: Nomenclatura: Dispositivo implantable, cardiaco (ISO/IEEE 11073-10103:2025) (Ratificada por la Asociación Española de Normalización en noviembre de 2025.)

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Standard number:UNE EN ISO/IEEE 11073-10103:2025
Pages:147
Released:2025-11-01
Status:Standard
DESCRIPTION

UNE EN ISO/IEEE 11073-10103:2025

1.1 Scope This standard extends the base nomenclature provided in ISO/IEEE 11073-10101:20206 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 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/IEEE 11073-10201 [B2]7) or with other standards, such as Health Level Seven International (HL7). 1.2 Purpose This standard addresses the need for an openly defined, independent standard for representing information collected from industry-wide implantable cardiac devices. A broader intent is to enable a standards-based exchange of implantable cardiac device information between vendor s proprietary interrogation systems and clinic electronic medical record systems.