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MSZ EN ISO/IEEE 11073-10404:2023

Dokumentumazonosító

181917

Cím

Egészségügyi informatika. Az eszközök interoperabilitása. 10404. rész: Személyi egészségügyi eszközök kommunikációja. Eszközönkénti részletezés. Pulzoximéter (ISO/IEEE 11073-10404:2022)

Angol cím

Health informatics. Device interoperability. Part 10404: Personal health device communication. Device specialization. Pulse oximeter (ISO/IEEE 11073-10404:2022)

Alkalmazási terület

1. Overview 1.1 Scope Within the context of the ISO/IEEE 11073 family of standards for device communication, this standard establishes a normative definition of communication between personal telehealth pulse oximeter devices and compute engines (e.g., cell phones, personal computers, personal health appliances, set top boxes) in a manner that enables plug-and-play (PnP) interoperability. It leverages appropriate portions of existing standards including ISO/IEEE 11073 terminology, information models, application profile standards, and transport standards. It specifies the use of specific term codes, formats, and behaviors in telehealth environments restricting optionality in base frameworks in favor of interoperability. This standard defines a common core of communication functionality for personal telehealth pulse oximeters. 1.2 Purpose This standard addresses a need for an openly defined, independent standard for controlling information exchange to and from personal health devices (PHDs) and compute engines (e.g., cell phones, personal computers, personal health appliances, set top boxes). Interoperability is key to growing the potential market for these devices and enabling people to be better informed participants in the management of their health. 1.3 Context See IEEE Std 11073-20601-2019™2 for an overview of the environment within which this standard is written. This standard, IEEE Std 11073-10404, defines the device specialization for the pulse oximeter, being a specific agent type, and provides a description of the device concepts, its capabilities, and its implementation according to this standard. This standard is based on IEEE Std 11073-20601-2019, which in turn draws information from both ISO/IEEE 11073-10201:2004 [B6]3 and ISO/IEEE 11073-20101:2004 [B7]. The medical device encoding rules (MDER) used within this standard are fully described in IEEE Std 11073-20601-2019. This standard defines specialized nomenclature codes that will be collected in IEEE Std 11073-10101-2019™. Between this standard, IEEE Std 11073-10101-2019, IEEE Std 11073-20601-2019 and other IEEE Std 11073-104xx, all required nomenclature codes for implementation are documented. New codes may be defined in newer versions / revisions of each of these documents. In the case of a conflict, where one term code has been assigned to two separate semantic concepts with different RefIDs, in general the oldest definition that is in actual use should take precedence. The same policy applies when one RefID has two different code values assigned in different specifications. The resolution of such conflicts will be determined through joint action by the responsible work groups and other stakeholders and any corrective action published as corrigenda. NOTE—In this standard, ISO/IEEE P11073-104zz is used to refer to the collection of device specialization standards that utilize IEEE Std 11073-20601-2019, where zz can be any number from 01 to 99, inclusive.4

ICS

35.240.80 Informatikai alkalmazások az egészségügyben

Műszaki Bizottság

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angol

Az érvényesség kezdete

2023-07-01

Forrás

idt ISO/IEEE 11073-10404:2022; idt EN ISO/IEEE 11073-10404:2022

Előd

MSZ EN ISO 11073-10404:2011

Utód

Módosítás

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