EN ISO 11073-10417:2014

Health informatics - Personal health device communication - Part 10417: Device specialization - Glucose meter (ISO/IEEE 11073-10417:2014, Corrected version 2014-06-01)

Within the context of the ISO/IEEE 11073 family of standards for device communication, ISO/IEEE 11073-10417:2014 establishes a normative definition of communication between personal telehealth glucose meter devices and computer engines (e.g. cell phones, personal computers, personal health appliances and set top boxes) in a manner that enables plug-and-play interoperability. Appropriate portions of existing standards are leveraged, including ISO/IEEE 11073 terminology, information models, application profile standards, and transport standards. The use of specific term codes, formats and behaviours in telehealth environments restricting optionality in base frameworks in favour of interoperability are specified. A common core of communication functionality for personal telehealth glucose meters is defined in ISO/IEEE 11073-10417:2014.

Medizinische Informatik - Kommunikation von Geräten für die persönliche Gesundheit - Teil 10417: Gerätespezifikation: Blutzuckermessgerät (ISO/IEEE 11073-10417:2014, korrigierte Fassung 2014-06-01)

Informatique de santé - Communication entre dispositifs médicaux sur le site des soins - Partie 10417: Spécialisation des dispositifs - Glucomètre (ISO/IEEE 11073-10417:2014, Version corrigée 2014-06-01)

Dans le contexte de la famille de normes ISO/IEEE 11073 relatives à la communication entre des dispositifs, la présente norme établit une définition normative de la communication entre des dispositifs glucomètres personnels de télésanté et des moteurs informatiques (par exemple des téléphones cellulaires, des ordinateurs personnels, des équipements personnels de santé et des boîtiers décodeurs) d'une manière qui permet une interopérabilité du type prêt à l'emploi. Elle s'appuie sur les parties appropriées de normes existantes, y compris la terminologie, des modèles d'informations, des normes de profils d'applications et des normes de transport de l'ISO/IEEE 11073. Elle spécifie l'utilisation de codes, de formats et de comportements en termes spécifiques dans les environnements de télésanté, en limitant les choix à des cadres de travail de base en faveur de l'interopérabilité. L'ISO/IEEE 11073-10417:2014 définit un noyau commun de fonctionnalités de communication pour les glucomètres personnels de télésanté.

Zdravstvena informatika - Komunikacija osebnih medicinskih naprav - 10417. del: Specialne naprave - Glukometer (ISO 11073-10417:2014)

Ta standard v okviru skupine standardov za komunikacijo naprav ISO/IEEE 11073 določa normativno opredelitev komunikacije med osebnimi telemedicinskimi glukometri in upravljalnimi napravami (npr. mobilnimi telefoni, osebnimi računalniki, osebnimi medicinskimi napravami in digitalnimi sprejemniki) na način, ki omogoča interoperabilnost s takojšnjim učinkom („vstavi in poženi“). Standard temelji na ustreznih delih obstoječih standardov, vključno s terminologijo iz standarda ISO/IEEE 11073, informacijskimi modeli, standardi za profile aplikacije in standardi za prevoz. Določa uporabo posebnih kod izrazov, formatov in vedenj v telemedicinskih okoljih, kjer v korist interoperabilnosti omejuje izbirnost osnovnih okvirov. Ta standard določa skupno jedro komunikacijske funkcionalnosti za osebne telemedicinske glukometre.

General Information

• Status: Withdrawn
• Publication Date: 04-Mar-2014
• Withdrawal Date: 16-May-2017
• ICS: 35.240.80 - IT applications in health care technology
• Technical Committee: CEN/TC 251 - Medical informatics
• Drafting Committee: CEN/TC 251/WG 2 - Terminology and knowledge representation
• Current Stage: 9960 - Withdrawal effective - Withdrawal
• Completion Date: 17-May-2017
• Ref Project: SIST EN ISO 11073-10417:2014 - Health informatics - Personal health device communication - Part 10417: Device specialization - Glucose meter (ISO 11073-10417:2014)

Relations

• Replaces: EN ISO 11073-10417:2011 - Health informatics - Personal health device communication - Part 10417: Device specialization - Glucose meter (ISO/IEEE 11073-10417:2010)
• Effective Date: 08-Jun-2022
• Replaced By: EN ISO 11073-10417:2017 - Health informatics - Personal health device communication - Part 10417: Device specialization - Glucose meter (ISO/IEEE 11073-10417:2017)
• Effective Date: 24-May-2017

Standards Content (Sample)

SLOVENSKI STANDARD
01-julij-2014
1DGRPHãþD
SIST EN ISO 11073-10417:2011
Zdravstvena informatika - Komunikacija osebnih medicinskih naprav - 10417. del:
Specialne naprave - Glukometer (ISO 11073-10417:2014)
Health informatics - Personal health device communication - Part 10417: Device
specialization - Glucose meter (ISO 11073-10417:2014)
Medizinische Informatik - Kommunikation von Geräten für die persönliche Gesundheit -
Teil 10417: Gerätespezifikation: Blutzuckermessgerät (ISO 11073-10417:2014)
Informatique de santé - Communication entre dispositifs de santé personnels - Partie
10417: Spécialisation des dispositifs: Glucomètre (ISO 11073-10417:2014)
Ta slovenski standard je istoveten z: EN ISO 11073-10417:2014
ICS:
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EUROPEAN STANDARD
EN ISO 11073-10417
NORME EUROPÉENNE
EUROPÄISCHE NORM
March 2014
ICS 35.240.80 Supersedes EN ISO 11073-10417:2011
English Version
Health informatics - Personal health device communication - Part
10417: Device specialization - Glucose meter (ISO/IEEE 11073-
10417:2014, Corrected version 2014-05-01)
Informatique de santé - Communication entre dispositifs Medizinische Informatik - Kommunikation von Geräten für
médicaux sur le site des soins - Partie 10417: die persönliche Gesundheit - Teil 10417:
Spécialisation des dispositifs - Glucomètre (ISO/IEEE Gerätespezifikation: Blutzuckermessgerät (ISO/IEEE
11073-10417:2014, Version corrigée 2014-05-01) 11073-10417:2014, korrigierte Fassung 2014-05-01)
This European Standard was approved by CEN on 14 December 2013.

CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European
Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national
standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member.

This European Standard exists in three official versions (English, French, German). A version in any other language made by translation
under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same
status as the official versions.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania,
Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United
Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2014 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 11073-10417:2014 E
worldwide for CEN national Members.

Contents Page
Foreword .3
Foreword
This document (EN ISO 11073-10417:2014) has been prepared by Technical Committee ISO/TC 215 “Health
informatics” in collaboration with Technical Committee CEN/TC 251 “Health informatics” the secretariat of
which is held by NEN.
This European Standard shall be given the status of a national standard, either by publication of an identical
text or by endorsement, at the latest by September 2014, and conflicting national standards shall be
withdrawn at the latest by September 2014.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN ISO 11073-10417:2011.
According to the CEN-CENELEC Internal Regulations, the national standards organizations of the following
countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech
Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece,
Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal,
Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom.
Endorsement notice
The text of ISO/IEEE 11073-10417:2014, Corrected version 2014-05-01 has been approved by CEN as
INTERNATIONAL ISO/IEEE
STANDARD 11073-
6HFRQG edition
201
Health informatics — Personal health
device communication —
Part 10417:
Device specialization: Glucose meter
Informatique de santé — Communication entre dispositifs de santé
personnels
Partie 10417: Spécialisation des dispositifs: Glucomètre

Reference number
ISO/IEEE 11073-10417:2013(E)
©
IEEE 2013
ISO/IEEE 11073-10417:2013(E)
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ISO version published 2013
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ii © IEEE 2013 – All rights reserved

ISO/IEEE 11073-10417:2013(E)
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies
(ISO member bodies). The work of preparing International Standards is normally carried out through ISO
technical committees. Each member body interested in a subject for which a technical committee has been
established has the right to be represented on that committee. International organizations, governmental and
non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the International
Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
IEEE Standards documents are developed within the IEEE Societies and the Standards Coordinating
Committees of the IEEE Standards Association (IEEE-SA) Standards Board. The IEEE develops its standards
through a consensus development process, approved by the American National Standards Institute, which
brings together volunteers representing varied viewpoints and interests to achieve the final product. Volunteers
are not necessarily members of the Institute and serve without compensation. While the IEEE administers the
process and establishes rules to promote fairness in the consensus development process, the IEEE does not
independently evaluate, test, or verify the accuracy of any of the information contained in its standards.
The main task of technical committees is to prepare International Standards. Draft International Standards
adopted by the technical committees are circulated to the member bodies for voting. Publication as an
International Standard requires approval by at least 75 % of the member bodies casting a vote.
Attention is called to the possibility that implementation of this standard may require the use of subject matter
covered by patent rights. By publication of this standard, no position is taken with respect to the existence or
validity of any patent rights in connection therewith. ISO/IEEE is not responsible for identifying essential
patents or patent claims for which a license may be required, for conducting inquiries into the legal validity or
scope of patents or patent claims or determining whether any licensing terms or conditions provided in
connection with submission of a Letter of Assurance or a Patent Statement and Licensing Declaration Form, if
any, or in any licensing agreements are reasonable or non-discriminatory. Users of this standard are expressly
advised that determination of the validity of any patent rights, and the risk of infringement of such rights, is
entirely their own responsibility. Further information may be obtained from ISO or the IEEE Standards
Association.
ISO/IEEE 11073-10417 was prepared by the Substations Committee of the IEEE Power Engineering Society
of the IEEE (as IEEE 1686-2007). It was adopted by Technical Committee ISO/TC 215, Respiratory and
anaesthetic equipment, in parallel with its approval by the ISO member bodies, under the “fast-track
procedure” defined in the Partner Standards Development Organization cooperation agreement between ISO
and IEEE. IEEE is responsible for the maintenance of this document with participation and input from ISO
member bodies.
ISO/IEEE 11073 consists of the following parts, under the general title Health informatics — Personal health
device communication (text in parentheses gives a variant of subtitle):
 Part 00103: Overview
 Part 10101: (Point-of-care medical device communication) Nomenclature
 Part 10102: (Point-of-care medical device communication) Nomenclature — Annotated ECG
 Part 10103: (Point-of-care medical device communication) — Nomenclature — Implantable device,
cardiac
 Part 10201: (Point-of-care medical device communication) Domain information model
 Part 10404: Device specialization — Pulse oximeter
© IEEE 2013 – All rights reserved iii

ISO/IEEE 11073-10417:2013(E)
 Part 10406: Device specialization — Basic electrocardiograph (ECG) (1- to 3-lead ECG)
 Part 10407: Device specialization — Blood pressure monitor
 Part 10408: Device specialization — Thermometer
 Part 10415: Device specialization — Weighing scale
 Part 10417: Device specialization — Glucose meter
 Part 10418: Device specialization — International Normalized Ratio (INR) monitor
 Part 10420: Device specialization — Body composition analyzer
 Part 10421: Device specialization — Peak expiratory flow monitor (peak flow)
 Part 10441: Device specialization — Cardiovascular fitness and activity monitor
 Part 10471: Device specialization — Independant living activity hub
 Part 10472: Device specialization — Medication monitor
 Part 20101: (Point-of-care medical device communication) Application profiles — Base standard
 Part 20601: Application profile — Optimized exchange protocol
 Part 30200: (Point-of-care medical device communication) Transport profile — Cable connected
 Part 30300: (Point-of-care medical device communication) Transport profile — Infrared wireless
 Part 30400: (Point-of-care medical device communication) Interface profile — Cabled Ethernet
 Part 90101: (Point-of-care medical device communication) Analytical instruments — Point-of-care test
 Part 91064: (Standard communication protocol) Computer-assisted electrocardiography
— Part 92001: (Medical waveform format) — Encoding rules
iv © IEEE 2013 – All rights reserved

Health Informatics—Personal health device communication

Part 10417: Device specialization—
Glucose meter
IEEE Engineering in Medicine and Biology Society

Sponsored by the
IEEE 11073™ Standards Committee

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IEEE Std 11073-10417™-2011
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IEEE Std 11073-10417 -2011
(Revision of
IEEE Std 11073-10417-2009)
Health informatics—Personal health device communication
Part 10417: Device specialization—
Glucose meter
Sponsor
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of the
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Abstract: Within the context o
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