EN ISO/IEEE 11073-10425:2025
(Main)Health informatics - Device interoperability - Part 10425: Personal Health Device Communication - Device Specialization- Continuous Glucose Monitor (CGM) (ISO/IEEE 11073-10425:2024)
Health informatics - Device interoperability - Part 10425: Personal Health Device Communication - Device Specialization- Continuous Glucose Monitor (CGM) (ISO/IEEE 11073-10425:2024)
This standard establishes a normative definition of communication between personal health continuous glucose monitor (CGM) devices (agents) and managers (e.g., cell phones, personal computers, personal health appliances, set top boxes) in a manner that enables plug-and-play interoperability. It leverages work done in other ISO/IEEE 11073 standards including existing terminology, information profiles, 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 of CGM devices. In this context, CGM refers to the measurement of the level of glucose in the body on a regular (typically 5 minute) basis through a sensor continuously attached to the person.
Medizinische Informatik - Interoperabilität von Geräten - Teil 10425: Kommunikation von Geräten für die persönliche Gesundheit - Gerätespezifikation - Kontinuierlicher Glukose-Monitor (ISO/IEEE 11073-10425:2024)
Informatique de santé - Interopérabilité des dispositifs - Partie 10425: Communication entre dispositifs de santé personnels - Spécialisation des dispositifs - Glucomètre continu (CGM) (ISO/IEEE 11073-10425:2024)
La présente norme établit une définition normative de la communication entre des dispositifs (agents) et des gestionnaires de glucomètres continus (CGM) personnels de santé (par exemple des téléphones cellulaires, des ordinateurs personnels, des équipements personnels de santé, des boîtiers décodeurs) d’une manière qui permet une interopérabilité du type prêt à l’emploi. Elle s’appuie sur le travail réalisé dans d’autres normes ISO/IEEE 11073, y compris la terminologie, des modèles d’informations, des normes de profils d’applications et des normes de transport. 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. La présente norme définit un noyau commun de fonctionnalités de communication des dispositifs CGM. Dans ce contexte, CGM désigne la mesure du niveau de glucose dans l’organisme relevé régulièrement (généralement toutes les 5 minutes) par le biais d’un capteur relié en permanence à la personne.
Zdravstvena informatika - Interoperabilnost naprav - 10425. del: Komunikacija osebnih medicinskih naprav - Specialne naprave - Stalno spremljanje ravni glukoze (ISO/IEEE 11073-10425:2024)
General Information
- Status
- Published
- Publication Date
- 30-Sep-2025
- Technical Committee
- CEN/TC 251 - Medical informatics
- Current Stage
- 6060 - Definitive text made available (DAV) - Publishing
- Start Date
- 01-Oct-2025
- Completion Date
- 01-Oct-2025
Relations
- Effective Date
- 08-Nov-2023
Overview
EN ISO/IEEE 11073-10425:2025 (ISO/IEEE 11073-10425:2024) defines a normative, plug-and-play communication framework for Continuous Glucose Monitors (CGM) and their managers (e.g., smartphones, PCs, personal health appliances, set‑top boxes). As part of the ISO/IEEE 11073 family, this device specialization standard prescribes a common core of communication functionality, leveraging existing 11073 terminology, information models and transport/application profiles to enable interoperable telehealth and personal‑health device ecosystems.
Key technical topics and requirements
- Device‑manager communication model: Normative definition of how CGM agents and managers exchange data to support continuous glucose measurement workflows.
- Terminology and information profiles: Uses ISO/IEEE 11073 terminology and information models to ensure consistent semantics across vendors.
- Restricted optionality for interoperability: Specifies required term codes, formats and behaviors and reduces optional choices in base frameworks to improve plug‑and‑play compatibility.
- Data formats and behaviors: Defines standardized term codes, attribute handling and message behaviors for CGM use cases (e.g., periodic sensor glucose reporting).
- Protocol/version and nomenclature management: Aligns nomenclature-version with protocol-version and clarifies precedence among 10101, 20601, 104xx and this device specialization.
- Normative references: References other standards such as IEEE Std 11073-20601 (device communication framework) and ISO/IEEE 11073-10101 (nomenclature) as part of the normative baseline.
- Telehealth focus: Emphasizes behaviors suitable for remote monitoring and personal health device scenarios, including common reporting cadence (typically ~5 minutes for CGM).
Practical applications and users
Who benefits:
- Medical device manufacturers building CGM sensors or transmitters seeking standardized, interoperable connectivity.
- Mobile and software developers integrating CGM data into apps, cloud services or electronic health records (EHRs).
- Healthcare providers and telehealth platforms needing reliable, standardized CGM feeds for remote monitoring and decision support.
- Test labs and regulators evaluating device conformance, safety and interoperability. Practical uses include plug‑and‑play pairing of CGM devices with smartphones, secure streaming of glucose data to health apps and EHRs, and consistent data exchange for clinical monitoring or research.
Related standards
- ISO/IEEE 11073 family (device communication series)
- IEEE Std 11073‑20601 (agent/manager framework)
- ISO/IEEE 11073‑10101 (nomenclature)
- Other ISO/IEEE 11073‑104xx device specializations
Note: Implementers should review the normative references and patent notices in the standard text before deployment. Keywords: continuous glucose monitor, CGM, IEEE 11073‑10425, medical device communication, personal health devices, device interoperability, telehealth, plug-and-play.
Frequently Asked Questions
EN ISO/IEEE 11073-10425:2025 is a standard published by the European Committee for Standardization (CEN). Its full title is "Health informatics - Device interoperability - Part 10425: Personal Health Device Communication - Device Specialization- Continuous Glucose Monitor (CGM) (ISO/IEEE 11073-10425:2024)". This standard covers: This standard establishes a normative definition of communication between personal health continuous glucose monitor (CGM) devices (agents) and managers (e.g., cell phones, personal computers, personal health appliances, set top boxes) in a manner that enables plug-and-play interoperability. It leverages work done in other ISO/IEEE 11073 standards including existing terminology, information profiles, 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 of CGM devices. In this context, CGM refers to the measurement of the level of glucose in the body on a regular (typically 5 minute) basis through a sensor continuously attached to the person.
This standard establishes a normative definition of communication between personal health continuous glucose monitor (CGM) devices (agents) and managers (e.g., cell phones, personal computers, personal health appliances, set top boxes) in a manner that enables plug-and-play interoperability. It leverages work done in other ISO/IEEE 11073 standards including existing terminology, information profiles, 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 of CGM devices. In this context, CGM refers to the measurement of the level of glucose in the body on a regular (typically 5 minute) basis through a sensor continuously attached to the person.
EN ISO/IEEE 11073-10425:2025 is classified under the following ICS (International Classification for Standards) categories: 35.240.80 - IT applications in health care technology. The ICS classification helps identify the subject area and facilitates finding related standards.
EN ISO/IEEE 11073-10425:2025 has the following relationships with other standards: It is inter standard links to EN ISO 11073-10425:2019. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
You can purchase EN ISO/IEEE 11073-10425:2025 directly from iTeh Standards. The document is available in PDF format and is delivered instantly after payment. Add the standard to your cart and complete the secure checkout process. iTeh Standards is an authorized distributor of CEN standards.
Standards Content (Sample)
SLOVENSKI STANDARD
01-december-2025
Nadomešča:
SIST EN ISO 11073-10425:2019
Zdravstvena informatika - Interoperabilnost naprav - 10425. del: Komunikacija
osebnih medicinskih naprav - Specialne naprave - Stalno spremljanje ravni
glukoze (ISO/IEEE 11073-10425:2024)
Health informatics - Device interoperability - Part 10425: Personal Health Device
Communication - Device Specialization- Continuous Glucose Monitor (CGM) (ISO/IEEE
11073-10425:2024)
Medizinische Informatik - Interoperabilität von Geräten - Teil 10425: Kommunikation von
Geräten für die persönliche Gesundheit - Gerätespezifikation - Kontinuierlicher Glukose-
Monitor (ISO/IEEE 11073-10425:2024)
Informatique de santé - Interopérabilité des dispositifs - Partie 10425: Communication
entre dispositifs de santé personnels - Spécialisation des dispositifs - Glucomètre
continu (CGM) (ISO/IEEE 11073-10425:2024)
Ta slovenski standard je istoveten z: EN ISO/IEEE 11073-10425:2025
ICS:
11.040.55 Diagnostična oprema 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.
EN ISO/IEEE 11073-
EUROPEAN STANDARD
NORME EUROPÉENNE
EUROPÄISCHE NORM
October 2025
ICS 35.240.80 Supersedes EN ISO 11073-10425:2019
English Version
Health informatics - Device interoperability - Part 10425:
Personal Health Device Communication - Device
Specialization- Continuous Glucose Monitor (CGM)
(ISO/IEEE 11073-10425:2024)
Informatique de santé - Interopérabilité des dispositifs Medizinische Informatik - Interoperabilität von
- Partie 10425: Communication entre dispositifs de Geräten - Teil 10425: Kommunikation von Geräten für
santé personnels - Spécialisation des dispositifs - die persönliche Gesundheit - Gerätespezifikation -
Glucomètre continu (CGM) (ISO/IEEE 11073- Kontinuierlicher Glukose-Monitor (ISO/IEEE 11073-
10425:2024) 10425:2024)
This European Standard was approved by CEN on 30 September 2024.
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, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway,
Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye and
United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2025 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO/IEEE 11073-10425:2025 E
worldwide for CEN national Members.
Contents Page
European foreword . 3
European foreword
This document (EN ISO/IEEE 11073-10425:2025) 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 April 2026, and conflicting national standards shall be
withdrawn at the latest by April 2026.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN ISO 11073-10425:2019.
Any feedback and questions on this document should be directed to the users’ national standards
body/national committee. A complete listing of these bodies can be found on the CEN website.
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, France, Germany, Greece, Hungary, Iceland,
Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Republic of
North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye and the
United Kingdom.
Endorsement notice
The text of ISO/IEEE 11073-10425:2024 has been approved by CEN as EN ISO/IEEE 11073-
10425:2025 without any modification.
International
Standard
ISO/IEEE
11073-10425
Third edition
Health informatics — Device
2024-09
interoperability —
Part 10425:
Personal health device
communication — Device
specialization — Continuous
Glucose Monitor (CGM)
Informatique de santé — Interopérabilité des dispositifs —
Partie 10425: Communication entre dispositifs de santé personnels
— Spécialisation des dispositifs — Glucomètre continu (CGM)
Reference number
ISO/IEEE 11073-10425:2024(en) © IEEE 2024
ISO/IEEE 11073-10425:2024(en)
© IEEE 2024
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ISO/IEEE 11073-10425:2024(en)
Foreword
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ISO/IEEE 11073-10425 was prepared by the IEEE 11073 Standards Committee of the IEEE Engineering in
Medicine and Biology Society (as IEEE Std 11073-10425) and drafted in accordance with its editorial rules. It
was adopted, under the “fast-track procedure” defined in the Partner Standards Development Organization
cooperation agreement between ISO and IEEE, by Technical Committee ISO/TC 215, Health informatics.
This third edition cancels and replaces the second edition (ISO/IEEE 11073-10425:2019), which has been
technically revised.
The main changes are as follows:
— updated Normative Reference to refer to IEEE Std 11073-20601-2019;
— updated version of this device specialization;
— updated the association details based on new version;
— updated the wording in 6.3 regarding the Observational;
— added some text to 6.12 to further elaborate the DIM extensibility rule;
— corrected the use condition of GET MDS at E.4.1;
© IEEE 2024 – All rights reserved
iii
ISO/IEEE 11073-10425:2024(en)
— updated the text in 8.5.2 regarding attribute-id-list, in order to be compliant with
20601-V4;
— added 4.3, Compliance with other standards;
— removed the year in bibliography to represent the latest version;
— updated the bit example in E.4.3 by inserting the Mds-Time-Info into MDS;
— made the ISO/IEEE 11073-10101 as normative reference;
— updated the wording at 1.3 and 4.1 regarding the precedence of nomenclature between
10101, 20601, 104xx and this standard;
— updated the usage of nomenclature-version. Tied it with the corresponding
protocol-version;
— updated the examples in Annex E using protocol-version4.
A list of all parts in the ISO 11073 series can be found on the ISO website.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www.iso.org/members.html.
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ISO/IEEE 11073-10425:2024(en)
Abstract: Within the context of the ISO/IEEE 11073 family of standards for device communication, a
normative definition of the communication between continuous glucose monitor (CGM) devices and
managers (e.g., cell phones, personal computers, personal health appliances, set top boxes), in a manner that
enables plug-and-play interoperability, is established in this standard. It leverages appropriate portions of
existing standards including ISO/IEEE 11073 terminology and information models. 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
of CGM devices. In this context, CGM refers to the measurement of the level of glucose in the body on a regular
(typically 5 minute) basis through a sensor continuously attached to the person.
Keywords: continuous glucose monitor, IEEE 11073-10425™, medical device communication, personal health
devices
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Participants
At the time this IEEE standard was submitted to the IEEE SA Standards Board for approval, the Personal Health Devices
Working Group had the following membership:
Daidi Zhong, Chair
Malcolm Clarke, Vice-Chair
Raymond Krasinski, Secretary
Karsten Aalders Chia-Chin Chong Raul Gonzalez Gomez
Charles R. Abbruscato Jinhan Chung Chris Gough
Nabil Abujbara John A. Cogan Channa Gowda
Maher Abuzaid John T. Collins Charles M. Gropper
James Agnew Cory Condek Amit Gupta
Manfred Aigner Todd H. Cooper Jeff Guttmacher
Jorge Alberola Sandra Costanzo Rasmus Haahr
David Aparisi Douglas Coup Christian Habermann
Lawrence Arne Nigel Cox Michael Hagerty
Diego B. Arquillo Hans Crommenacker Jerry Hahn
Serafin Arroyo Tomio Crosley Robert Hall
Muhammad Asim Allen Curtis Shu Han
Kit August Jesús Daniel Trigo Nathaniel Hamming
Doug Baird David Davenport Rickey L. Hampton
David Baker Russell Davis Sten Hanke
Anindya Bakshi Sushil K. Deka Aki Harma
Ananth Balasubramanian Ciro de la Vega Jordan Hartmann
Sunlee Bang Jim Dello Stritto Kai Hassing
M. Jonathan Barkley Kent Dicks Avi Hauser
Gilberto Barrón Hyoungho Do Nathaniel Heintzman
David Bean Fangjie Dong Charles Henderson
John Bell Jonathan Dougherty Jun-Ho Her
Olivia Bellamou-Huet Xiaolian Duan Timothy L. Hirou
Rudy Belliardi Sourav Dutta Allen Hobbs
Daniel Bernstein Jakob Ehrensvard Alex Holland
George A. Bertos Fredrik Einberg Arto Holopainen
Chris Biernacki Javier Escayola Calvo Kris Holtzclaw
Ola Björsne Mark Estes Robert Hoy
Thomas Blackadar Leonardo Estevez Anne Huang
Thomas Bluethner Michael Faughn Guiling Huang
Douglas P. Bogia Bosco T. Fernandes Haofei Huang
Xavier Boniface Christoph Fischer Zhiyong Huang
Shannon Boucousis Morten Flintrup David Hughes
Lyle G. Bullock, Jr. Russell Foster Robert D. Hughes
Bernard Burg Eric Freudenthal Jiyoung Huh
Chris Burns Matthias Frohner Hugh Hunter
Jeremy Byford-Rew Kenneth Fuchs Philip O. Isaacson
Satya Calloji Jing Gao Atsushi Ito
Carole C. Carey Marcus Garbe Michael Jaffe
Craig Carlson John Garguilo Praduman Jain
Santiago Carot-Nemesio Liang Ge Zongbo Jiang
Seungchul Chae Rick Geimer Hu Jin
Yao Chen Igor Gejdos Danny Jochelson
Jing Cheng Ferenc Gerbovics Akiyoshi Kabe
Peggy Chien Alan Godfrey Steve Kahle
David Chiu Nicolae Goga Tomio Kamioka
Jinyong Choi Julian Goldman James J. Kang
© IEEE 2024 – All rights reserved
ix
ISO/IEEE 11073-10425:2024(en)
Kei Kariya Carsten Mueglitz Sid Shaw
Andy Kaschl Soundharya Nagasubramanian Frank Shen
Junzo Kashihara Alex Neefus Min Shih
Ralph Kent Trong-Nghia Nguyen-Dobinsky Mazen Shihabi
Laurie M. Kermes Michael E. Nidd Redmond Shouldice
Sanjay R. Kharche Jim Niswander Sternly K. Simon
Ahmad Kheirandish Hiroaki Niwamoto Marjorie Skubic
Junhyung Kim Thomas Norgall Robert Smith
Minho Kim Yoshiteru Nozoe Ivan Soh
Min-Joon Kim Abraham Ofek Motoki Sone
Taekon Kim Brett Olive Emily Sopensky
Tetsuya Kimura BegonyaOtal Rajagopalan Srinivasan
Michael J. Kirwan Marco Paleari Nicholas Steblay
Alfred Kloos Bud Panjwani Lars Steubesand
Edward Koch Carl Pantiskas John (Ivo) Stivoric
Jeongmee Koh Harry P. Pappas Hermanni Suominen
Jean-Marc Koller Hanna Park Lee Surprenant
John Koon Jong-Tae Park Ravi Swami
Patty Krantz Myungeun Park Ray Sweidan
Alexander Kraus Phillip E. Pash Na Tang
Ramesh Krishna TongBi Pei Haruyuyki Tatsumi
Geoffrey Kruse Soren Petersen Isabel Tejero
Falko Kuester James Petisce Tom Thompson
Rafael Lajara Peter Piction Jonas Tirén
Pierre Landau Michael Pliskin Janet Traub
Jaechul Lee Varshney Prabodh Gary Tschautscher
JongMuk Lee Jeff Price Masato Tsuchid
Kyong Ho Lee Harald Prinzhorn Ken Tubman
Rami Lee Lifei Qian Akib Uddin
Sungkee Lee Harry Qiu Sunil Unadkat
Woojae Lee Tanzilur Rahman Fabio Urbani
Jing Li Lin Ran Philipp Urbauer
Qiong Li Phillip Raymond Laura Vanzago
Xiangchen Li Terrie Reed Alpo Värri
Patrick Lichter Barry Reinhold Andrei Vasilateanu
Jisoon Lim Brian Reinhold Dalimar Velez
Wei-Jung Lo Melvin I. Reynolds Martha Velezis
Charles Lowe John G. Rhoads Rudi Voon
Don Ludolph Jeffrey S. Robbins Isobel Walker
Ling Luo Chris Roberts David Wang
Christian Luszick Moskowitz Robert Jerry P. Wang
Bob MacWilliams Stefan Robert Shiwei Wang
Srikkanth Madhurbootheswaran Scott M. Robertson Yao Wang
Miriam L. Makhlouf Timothy Robertson Yi Wang
M. Sabarimalai Manikandan Sean Rocke Steve Warren
Romain Marmot David Rosales Fujio Watanabe
Sandra Martinez Bill Saltzstein Toru Watsuji
Miguel Martínez de EsproncedaCámara Giovanna Sannino Kathleen Wible
Peter Mayhew Jose A. Santos-Cadenas
Jim McCain Stefan Sauermann Paul Williamson
LászlóMeleg John Sawyer Jia-Rong Wu
Alexander Mense Alois Schloegl Will Wykeham
Behnaz Minaei Paul S. Schluter Ariton Xhafa
Jinsei Miyazaki Mark G. Schnell Ricky Yang
Madhu Mohan Richard A. Schrenker Melanie S. Yeung
Erik Moll Antonio Scorpiniti Qiang Yin
Darr Moore KwangSeok Seo Done-Sik Yoo
Chris Morel Riccardo Serafin Zhi Yu
© IEEE 2024 – All rights reserved
x
ISO/IEEE 11073-10425:2024(en)
Jianchao Zeng Liang Zheng Miha Zoubek
Jason Zhang Daidi Zhong Szymon Zyskoter
Zerui Zhang Yuanhong Zhong
Shiwei Zhao Qing Zhou
The following members of the individual balloting committee voted on this standard. Balloters may have voted for approval,
disapproval, or abstention.
Robert Aiello Charles M. Gropper Bansi Patel
Cheryl Alexander Wang Werner Hoelzl Scott M. Robertson
Bjoern Andersen Piotr Karocki Stefan Schlichting
Pradeep Balachandran Stuart Kerry Walter Struppler
Malcolm Clarke Raymond Krasinski John Vergis
Javier Espina H. Moll Yu Yuan
Michael Faughn Rajesh Murthy Oren Yuen
Kenneth Fuchs Daidi Zhong
When the IEEE SA Standards Board approved this standard on 30 March 2023, it had the following membership:
David J. Law, Chair
Ted Burse, Vice Chair
Gary Hoffman, Past Chair
Konstantinos Karachalios, Secretary
Sara R. Biyabani Joseph S. Levy Paul Nikolich
Doug Edwards Howard Li Annette D. Reilly
Ramy Ahmed Fathy Johnny Daozhuang Lin Robby Robson
Guido R. Hiertz Gui Lin Lei Wang
Yousef Kimiagar Xiaohui Liu F. Keith Waters
Joseph L. Koepfinger* Kevin W. Lu Karl Weber
Thomas Koshy Daleep C. Mohla Philip B. Winston
John D. Kulick Andrew Myles Don Wright
*Member Emeritus
© IEEE 2024 – All rights reserved
xi
ISO/IEEE 11073-10425:2024(en)
Introduction
This introduction is not part of IEEE Std 11073-10425-2023, Health Informatics—Device Interoperability—Part 10425: Personal Health
Device Communication—Device Specialization—Continuous Glucose Monitor (CGM).
ISO/IEEE 11073 standards enable communication between medical devices and external computer systems. This document uses
the optimized framework created in ISO/IEEE 11073-20601 and describes a specific, interoperable communication approach for
continuous glucose monitors (CGMs). These standards align with, and draw on, the existing clinically focused standards to
provide support for communication of data from clinical or personal health devices (PHDs).
Information on references can be found in Clause 2.
© IEEE 2024 – All rights reserved
xii
ISO/IEEE 11073-10425:2024(en)
Contents
1. Overview . 1
1.1 Scope . 1
1.2 Purpose . 1
1.3 Word usage . 1
1.4 Context . 1
2. Normative references . 2
3. Definitions, acronyms, and abbreviations . 2
3.1 Definitions . 2
3.2 Acronyms and abbreviations . 3
4. Introduction to ISO/IEEE 11073 personal health devices (PHDs) . 4
4.1 General . 4
4.2 Introduction to ISO/IEEE 11073-20601 modeling constructs . 4
4.3 Compliance with other standards . 5
5. Glucose monitoring concepts and modalities . 5
5.1 General . 5
5.2 Device types . 6
5.3 CGM agent-to-manager communication . 7
5.4 Collected data . 7
5.5 Stored data . 9
6. Continuous glucose monitor (CGM) domain information model (DIM) . 9
6.1 Overview . 9
6.2 Class extensions . 9
6.3 Object instance diagram . 9
6.4 Types of configuration . 11
6.5 Profiles . 11
6.6 MDS object. 11
6.7 Numeric objects . 14
6.8 Real-time sample array objects. 24
6.9 Enumeration objects . 24
6.10 PM-store objects . 27
6.11 Scanner objects . 31
6.12 Class extension objects . 31
6.13 CGM information model extensibility rules . 31
7. CGM service model . 32
7.1 General . 32
7.2 Object access services . 32
7.3 Object access event report services . 34
8. CGM communication model . 34
8.1 Overview . 34
8.2 Communication characteristics . 34
8.3 Association procedure . 35
8.4 Configuring procedure . 36
8.5 Operating procedure . 38
8.6 Time synchronization . 39
© IEEE 2024 – All rights reserved
xiii
ISO/IEEE 11073-10425:2024(en)
9. Test associations . 39
9.1 Behavior with standard configuration . 39
9.2 Behavior with extended configurations . 39
10. Conformance . 39
10.1 Applicability . 39
10.2 Conformance specification . 39
10.3 Levels of conformance. 40
Annex A (informative) Bibliography . 46
Annex B (normative) Any additional ASN.1 definitions . 47
Annex C (normative) Allocation of identifiers . 51
Annex D (informative) Message sequence examples . 56
Annex E (informative) Protocol data unit examples. 58
Annex F (informative) Revision history . 67
© IEEE 2024 – All rights reserved
xiv
ISO/IEEE 11073-10425:2024(en)
Health Informatics—Device Interoperability
Part 10425:
Personal Health Device Communication—Device
Specialization—Continuous Glucose Monitor (CGM)
1. Overview
1.1 Scope
This standard establishes a normative definition of communication between personal health continuous glucose monitor (CGM)
devices (agents) and managers (e.g., cell phones, personal computers, personal health appliances, set top boxes) in a manner that
enables plug-and-play interoperability. It leverages work done in other ISO/IEEE 11073 standards including existing
terminology, information profiles, 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 of CGM devices. In this context, CGM refers to the
measurement of the level of glucose in the body on a regular (typically 5 minute) basis through a sensor continuously attached to
the person.
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 the key to growing the potential market for these devices and to enabling people to be better informed
participants in the management of their health.
1.3 Word usage
The word shall indicates mandatory requirements strictly to be followed in order to conform to the standard and from which no
2, 3
deviation is permitted (shall equals is required to).
The word should indicates that among several possibilities one is recommended as particularly suitable, without mentioning or
excluding others; or that a certain course of action is preferred but not necessarily required (should equals is recommended that).
The word may is used to indicate a course of action permissible within the limits of the standard (may equals is permitted to
...
EN ISO/IEEE 11073-10425:2025 표준은 개인 건강 지속적 포도당 모니터(CGM) 장치와 이를 관리하는 장치들 간의 통신에 대한 규범적 정의를 제공합니다. 이 표준은 플러그 앤 플레이 상호 운용성을 가능하게 하는 방식으로 통신을 설정하여, 셀폰, 개인용 컴퓨터, 개인 건강 기기 및 셋톱박스와 같은 여러 장치 간의 원활한 데이터 통신을 지원합니다. 이 표준의 큰 장점 중 하나는 다른 ISO/IEEE 11073 표준에서 수행된 작업을 활용하며, 기존의 용어, 정보 프로필, 응용 프로필 표준 및 전송 표준을 포함한다는 것입니다. 이를 통해 CGM 장치 간의 통신 기능의 공통 핵심을 정의하고, 원활한 상호 운용성을 위한 기본 프레임워크의 선택적 요소를 제한합니다. 이와 같은 제한은 다양한 기기 간의 호환성을 높여 사용자가 더 안정적으로 건강 데이터를 관리할 수 있도록 합니다. CGM 장치는 일반적으로 5분마다 인체의 포도당 수치를 측정하는 센서를 사용하여, 지속적으로 포도당 수치를 측정합니다. 이 표준은 이러한 기능을 수행하는 CGM 장치의 통신 방식을 명확히 규정함으로써, 의료 환경에서의 원격 진료가 효율적으로 이루어질 수 있도록 기여합니다. 전반적으로 EN ISO/IEEE 11073-10425:2025 표준은 개인 건강 관리의 필수적인 요소로 자리 잡고 있으며, 장치의 상호 운용성을 중심으로 한 혁신적인 접근 방식은 현대의료 기술 발전에 중요한 역할을 하고 있습니다.
標準文書「EN ISO/IEEE 11073-10425:2025」は、個人の健康管理における継続的なグルコースモニター(CGM)デバイスの通信に関する重要な基準を提供しています。この標準は、CGMデバイス(エージェント)とマネージャー(スマートフォン、パソコン、個人健康機器、セットトップボックスなど)との間の通信方法を規定しており、プラグアンドプレイの相互運用性を可能にするためのノーマティブな定義を確立しています。 この標準の強みは、既存のISO/IEEE 11073の他の標準に基づいており、用語、情報プロファイル、アプリケーションプロファイル標準、およびトランスポート標準の整合性を持たせている点です。特に、選択肢を制限することで基本フレームワークにおける相互運用性を促進しており、CGMデバイス間の通信機能の共通コアを定義しています。このアプローチは、テレヘルス環境での一貫した用語コード、フォーマット、動作を使用することを指定しており、より高い信頼性と使いやすさを実現しています。 さらに、CGMデバイスは、通常5分ごとに人体内のグルコースレベルを測定するセンサーを使用しており、この標準はそれに特化しています。このように、EN ISO/IEEE 11073-10425:2025は、政策立案者や技術者にとって不可欠なリソースであり、個人健康デバイスの相互運用性の向上を通じて、患者のケアの質を向上させることに寄与しています。
Die Norm EN ISO/IEEE 11073-10425:2025 ist ein bedeutendes Dokument im Bereich der Gesundheitsinformatik, das sich mit der Interoperabilität von Geräten beschäftigt. Sie definiert normativ die Kommunikation zwischen persönlichen Gesundheitsgeräten, insbesondere kontinuierlichen Glukosemonitoren (CGM), und Verwaltungsgeräten wie Mobiltelefonen, Personal Computern und anderen Gesundheitsgeräten. Der Fokus auf Plug-and-Play-Interoperabilität zeigt die Absicht, die Integration von CGM-Systemen in bestehende Infrastrukturen zu vereinfachen. Ein herausragendes Merkmal dieser Norm ist die Nutzung bereits erarbeiteter Standards aus anderen ISO/IEEE 11073-Dokumenten. Durch die Verwendung etablierter Terminologie, Informationsprofile und Anwendungsprofile wird die Konsistenz und Verständlichkeit der Kommunikation zwischen den Geräten gefördert. Dieses Vorgehen stärkt die Relevanz der Norm, da sie auf bewährten Grundlagen basiert und gleichzeitig spezifische Anforderungen an die Verwendung von Termincode, Formaten und Verhaltensweisen in Telehealth-Umgebungen festlegt. Ein wesentliches Ziel dieser Norm ist es, die Interoperabilität zu maximieren, indem sie die Optionalität im Basiskonzept einschränkt. Dies bedeutet, dass verschiedene Hersteller dazu ermutigt werden, die gleichen Kommunikationsprotokolle und -standards zu befolgen, wodurch Komplikationen und Inkompatibilitäten in der Nutzung von CGM-Geräten minimiert werden. Die definierte Kommunikationsfunktionalität schafft eine gemeinsame Grundlage, die sicherstellt, dass sämtliche CGM-Geräte effizient miteinander kommunizieren können. Die Norm behandelt die regelmäßige Messung des Glukosespiegels im Körper, was für das Management von Diabetes von zentraler Bedeutung ist. Indem sie eine klare und umfassende Richtschnur für die Kommunikation zwischen CGM-Geräten und deren Managementsystemen bereitstellt, trägt die EN ISO/IEEE 11073-10425:2025 entscheidend zur Verbesserung der Patientensicherheit und der Effektivität von Telehealth-Lösungen bei. Insgesamt stellt die Norm einen essenziellen Schritt in Richtung einer besseren Geräteinteroperabilität im Gesundheitswesen dar.
La norme EN ISO/IEEE 11073-10425:2025 établit une définition normative de la communication entre les dispositifs de surveillance continue de la glycémie (CGM) et les gestionnaires tels que les téléphones portables, les ordinateurs personnels et les appareils de santé personnels. Cette norme se distingue par son approche de l'interopérabilité "plug-and-play", ce qui en fait un outil essentiel pour les professionnels de la santé et les utilisateurs finaux souhaitant intégrer facilement des dispositifs de santé personnels dans des systèmes variés. L'un des principaux atouts de cette norme réside dans son intégration des travaux antérieurs réalisés dans d'autres normes ISO/IEEE 11073. En s'appuyant sur une terminologie existante, des profils d'information et des normes de transport, elle assure une continuité et une cohérence dans la communication entre divers dispositifs. Cela crée une efficacité opérationnelle qui est primordiale dans les environnements de télésanté. En spécifiant des codes de termes, des formats et des comportements précis, la norme limite l'optionnalité au sein des cadres de base, favorisant ainsi l'interopérabilité entre les dispositifs. Ce niveau de standardisation est crucial pour la mise en œuvre réussie des solutions de télésanté, car il garantit que tous les dispositifs peuvent communiquer de manière fluide, sans nécessiter de configurations complexes ou de développements supplémentaires. La définition d'une fonctionnalité de communication de base commune pour les dispositifs CGM renforce la pertinence de cette norme dans le domaine de l'informatique de santé. En offrant un cadre standardisé pour la mesure régulière des niveaux de glucose, elle facilite le suivi continu des patients et améliore la qualité des soins. En résumé, la norme EN ISO/IEEE 11073-10425:2025 représente une avancée significative vers une meilleure interconnexion des dispositifs de santé personnels, essentielle pour le développement futur de la télésanté et le bien-être des utilisateurs.
The standard EN ISO/IEEE 11073-10425:2025 provides a robust framework for ensuring effective communication between personal health continuous glucose monitor (CGM) devices and various management systems, such as cell phones and personal computers. Its primary focus is on device interoperability, specifically in telehealth environments, by establishing a normative definition that facilitates plug-and-play capabilities. One of the significant strengths of this standard lies in its comprehensive integration of previous ISO/IEEE 11073 standards, which provides a solid foundation of terminology, information profiles, and application frameworks. This integration ensures that stakeholders can leverage existing knowledge while focusing on the specific needs of CGM devices. By doing so, the standard aids in creating a cohesive system that supports seamless communication and functionality among diverse health technology products. Moreover, the emphasis on reducing optionality within the framework to promote interoperability is particularly noteworthy. By mandating certain term codes, formats, and behaviors, the standard substantially mitigates variability in CGM device interactions, leading to increased consistency and reliability in data exchange. This is crucial in healthcare settings, where accurate and timely glucose level monitoring can significantly impact patient outcomes. The scope of EN ISO/IEEE 11073-10425:2025 is also highly relevant as it specifies the continuous and regular measurement of glucose levels, reflecting the growing need for effective real-time monitoring of diabetic patients. Given the increasing integration of health devices into personal and clinical use, the relevance of this standard cannot be overstated; it supports healthcare professionals and patients in managing glycemic control, ultimately contributing to better health outcomes. In summary, the standard serves as a pivotal resource for advancing continuous glucose monitor (CGM) interoperability within health informatics. Its strengths lie in its foundational connections to earlier standards, its focus on reducing variability, and its relevance to modern healthcare practices, making it an essential tool for stakeholders aiming for enhanced device communication and patient care.










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