Health informatics - Device interoperability - Part 10101:Point-of-care medical device communication - Nomenclature (ISO/IEEE 11073-10101:2020)

This standard defines a nomenclature for communication of information from point-of-care medical
devices. Primary emphasis is placed on acute care medical devices and patient vital signs information. The
nomenclature also supports concepts in an object-oriented information model that is for medical device
communication.

Medizinische Informatik - Kommunikation patientennaher medizinischer Geräte - Teil 10101: Nomenklatur (ISO/IEEE 11073-10101:2020)

Informatique de santé - Interopérabilité des dispositifs - Partie 10101: Communication entre dispositifs médicaux sur le site des soins - Nomenclature (ISO/IEEE 11073-10101:2020)

La présente norme définit une nomenclature pour la communication d’informations à partir de dispositifs médicaux aux sites des soins. L’accent est mis principalement sur les dispositifs médicaux de soins actifs et les informations relatives aux signes vitaux du patient. La nomenclature prend également en charge les concepts dans un modèle d’information orienté objet destiné à la communication entre les dispositifs médicaux.

Zdravstvena informatika - Interoperabilnost naprav - 10101. del: Komunikacija medicinskih naprav na mestu oskrbe - Nomenklatura (ISO/IEEE 11073-10101:2020)

General Information

Status
Published
Public Enquiry End Date
26-Mar-2020
Publication Date
17-Jan-2021
Technical Committee
Current Stage
6060 - National Implementation/Publication (Adopted Project)
Start Date
07-Oct-2020
Due Date
12-Dec-2020
Completion Date
18-Jan-2021

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SLOVENSKI STANDARD
SIST EN ISO 11073-10101:2021
01-februar-2021
Nadomešča:
SIST EN ISO 11073-10101:2005
SIST EN ISO 11073-10101:2005/A1:2018
Zdravstvena informatika - Interoperabilnost naprav - 10101. del: Komunikacija
medicinskih naprav na mestu oskrbe - Nomenklatura (ISO/IEEE 11073-10101:2020)
Health informatics - Device interoperability - Part 10101:Point-of-care medical device
communication - Nomenclature (ISO/IEEE 11073-10101:2020)
Medizinische Informatik - Kommunikation patientennaher medizinischer Geräte - Teil
10101: Nomenklatur (ISO/IEEE 11073-10101:2020)
Informatique de santé - Interopérabilité des dispositifs - Partie 10101: Communication
entre dispositifs médicaux sur le site des soins - Nomenclature (ISO/IEEE 11073-
10101:2020)
Ta slovenski standard je istoveten z: EN ISO 11073-10101:2020
ICS:
01.040.35 Informacijska tehnologija. Information technology
(Slovarji) (Vocabularies)
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
SIST EN ISO 11073-10101:2021 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------
SIST EN ISO 11073-10101:2021

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SIST EN ISO 11073-10101:2021
EN ISO 11073-10101
EUROPEAN STANDARD
NORME EUROPÉENNE
September 2020
EUROPÄISCHE NORM
ICS 01.040.35; 35.240.80 Supersedes EN ISO 11073-10101:2005
English Version
Health informatics - Device interoperability - Part 10101:
Point-of-care medical device communication -
Nomenclature (ISO/IEEE 11073-10101:2020)
Informatique de santé - Interopérabilité des dispositifs Medizinische Informatik - Kommunikation
- Partie 10101: Communication entre dispositifs patientennaher medizinischer Geräte - Teil 10101:
médicaux sur le site des soins - Nomenclature Nomenklatur (ISO/IEEE 11073-10101:2020)
(ISO/IEEE 11073-10101:2020)
This European Standard was approved by CEN on 22 June 2020.
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, Turkey 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
© 2020 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 11073-10101:2020 E
worldwide for CEN national Members.

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SIST EN ISO 11073-10101:2021
EN ISO 11073-10101:2020 (E)
Contents Page
European foreword . 3

2

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SIST EN ISO 11073-10101:2021
EN ISO 11073-10101:2020 (E)
European foreword
This document (EN ISO 11073-10101:2020) 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 March 2021, and conflicting national standards shall
be withdrawn at the latest by March 2021.
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 11073-10101:2005.
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, Turkey and the
United Kingdom.
Endorsement notice
The text of ISO/IEEE 11073-10101:2020 has been approved by CEN as EN ISO 11073-10101:2020
without any modification.

3

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SIST EN ISO 11073-10101:2021

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SIST EN ISO 11073-10101:2021
ISO/IEEE
INTERNATIONAL
11073-10101
STANDARD
Second edition
2020-08
Health informatics — Device
interoperability —
Part 10101:
Point-of-care medical device
communication — Nomenclature
Informatique de santé — Interopérabilité des dispositifs —
Partie 10101: Communication entre dispositifs médicaux sur le site
des soins — Nomenclature
Reference number
ISO/IEEE 11073-10101:2020(E)
©
IEEE 2019

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SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)

COPYRIGHT PROTECTED DOCUMENT
© IEEE 2019
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
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Institute of Electrical and Electronics Engineers, Inc
3 Park Avenue, New York
NY 10016-5997, USA
Email: stds.ipr@ieee.org
Website: www.ieee.org
Published in Switzerland
ii © IEEE 2019 – All rights reserved

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SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(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
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electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted (see www.iso.org/directives).
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.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of any
patent rights identified during the development of the document will be in the Introduction and/or on the
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Any trade name used in this document is information given for the convenience of users and does not
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iso/foreword.html.
ISO/IEEE 11073-10101 was prepared by the IEEE 11073 Standards Committee of the IEEE
Engineering in Medicine and Biology Society (as IEEE Std 11073-10101-2019) 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 second edition cancels and replaces the first edition (ISO/IEEE 11073-10101:2004), which has been
technically revised. It also incorporates the Amendment ISO/IEEE 11073-10101:2004/Amd 1:2017.
A list of all parts in the ISO/IEEE 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.
© IEEE 2019 – All rights reserved iii

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SIST EN ISO 11073-10101:2021

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SIST EN ISO 11073-10101:2021
IEEE Std 11073-10101™-2019
(Revision of
ISO/IEEE 11073-10101:2004)
Health informatics—Point-of-care medical device communication
Part 10101: Nomenclature
Developed by the
IEEE 11073™ Standards Committee
of the
IEEE Engineering in Medicine and Biology Society
Approved 13 June 2019
IEEE SA Standards Board

---------------------- Page: 11 ----------------------
SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)
Abstract: Within the context of the ISO/IEEE 11073 family of standards for point-of-care (POC)
and personal health devices (PHD) medical device communication (MDC), this standard provides
the nomenclature that supports both the domain information model and service model
components of the standards family, as well as the semantic content exchanged with medical
devices. The nomenclature is specialized for patient vital signs information representation and
medical device informatics, with major areas including concepts for electrocardiograph (ECG),
haemodynamics, respiration, blood gas, urine, fluid-related metrics, and neurology, as well as
specialized units of measurement, general device events, alarms, and body sites. The standard
defines both the architecture and major components of the nomenclature, along with extensive
definitions for each conceptual area.
Keywords: codes, IEEE 11073-10101™, IHE PCD-01, independent living, information model,
medical device communication, nomenclature, ontology, patient, personal health devices, PHD,
POC, point-of-care, semantics, service model, terminology

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SNOMED is a registered trademark of the College of American Pathologists (http://www.cap.org).
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of the publisher.
2
Copyright © 2018 IEEE. All rights reserved.

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SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)
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3
Copyright © 2019 IEEE. All rights reserved.

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SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)

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Copyright © 2019 IEEE. All rights reserved.

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SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)

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5
Copyright © 2019 IEEE. All rights reserved.

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SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)

Participants
At the time this draft standard was approved by the IEEE SA Standards Board, the Point-of-Care Devices
Working Group had the following membership:
Malcolm Clarke, Chair
Paul Schluter, Vice Chair

Spencer Crosswy Kai Hassing Mathieu Roullet
Steven Dain Stefan Karl Stefan Schlichting
Michael Faughn Brian Reinhold Richard Tayrien
Kenneth Fuchs Melvin Reynolds Michi Tietz
Marcus Garbe John Rhoads Jan Wittenber
John Garguilo Daidi Zhong

The following members of the individual balloting committee voted on this standard. Balloters may have
voted for approval, disapproval, or abstention.

Bjoern Andersen Noriyuki Ikeuchi Paul Schluter
Keith Chow Atsushi Ito Walter Struppler
Malcolm Clarke Stefan Karl Ganesh Subramanian
David Fuschi Piotr Karocki Lisa Ward
Randall Groves Martin Kasparick Jan Wittenber
Kai Hassing H. Moll Oren Yuen
Werner Hoelzl Beth Pumo Daidi Zhong
Stefan Schlichting

When the IEEE SA Standards Board approved this standard on 13 June 2019, it had the following
membership:

Gary Hoffman, Chair
Ted Burse, Vice Chair
Jean-Philippe Faure, Past Chair
Konstantinos Karachalios, Secretary

Masayuki Ariyoshi Thomas Koshy Annette D. Reilly
Ted Burse John D. Kulick Dorothy Stanley
Stephen D. Dukes David J. Law Sha Wei
J. Travis Griffith Joseph Levy Phil Wennblom
Guido Hiertz Howard Li Philip Winston
Christel Hunter Xiaohui Liu Howard Wolfman
Thomas Koshy Kevin Lu Feng Wu
Joseph L. Koepfinger* Daleep Mohla Jingyi Zhou
Andrew Myles

*Member Emeritus

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Copyright © 2019 IEEE. All rights reserved.

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SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)
Introduction
This introduction is not part of IEEE Std 11073-10101-2019, Health informatics—Point-of-Care Medical Device
Communication—Nomenclature.
ISO/IEEE 11073 standards enable communication between medical devices and external computer
systems. They provide automatic and detailed electronic data capture of patient vital signs information and
device operational data. The primary goals are to
⎯ Provide real-time plug-and-play interoperability for patient-connected medical devices.
⎯ Facilitate the efficient exchange of vital signs and medical device data, acquired at the point-of-
care, in all health care environments.
“Real-time” means that data from multiple devices can be retrieved, time correlated, and displayed or
processed in fractions of a second. “Plug-and-play” means that all the clinician has to do is make the
connection — the systems automatically detect, configure, and communicate without any other human
interaction.
“Efficient exchange of medical device data” means that information that is captured at the point-of-care
(e.g., patient vital signs data) can be archived, retrieved, and processed by many different types of
applications without extensive software and equipment support, and without needless loss of information.
The standards focus on acute care devices, such as patient monitors, ventilators, infusion pumps, ECG
devices, etc, and personal health devices and systems. They comprise a family of standards that can be
layered together to provide connectivity optimized for the specific devices being interfaced.
IEEE Std 11073-10101 was originally published in 2004 in conjunction with the International Organization
for Standardization (ISO). In 2015, IEEE published an amendment that expanded the nomenclature and
definitions covered in the standard to reflect the continued innovation in medical device and system design.
This 2019 revision integrates the amendment into the original text and further updates and expands the
nomenclature and definitions.
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Copyright © 2019 IEEE. All rights reserved.

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SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)
Contents
1. Scope . 20
2. Normative references . 20
3. Terms, definitions, symbols, and abbreviated terms. 22
3.1 Terms and definitions . 22
3.2 Symbols and abbreviated terms . 22
4. Conformance . 25
5. Introduction to the standard . 25
6. Application . 25
7. Semantics. 26
7.1 Attribution . 26
7.2 Coding . 27
7.2.1 Co
...

SLOVENSKI STANDARD
oSIST prEN ISO 11073-10101:2020
01-marec-2020
Zdravstvena informatika - Komunikacija medicinskih naprav na mestu oskrbe -
10101. del: Nomenklatura (ISO/IEEE FDIS 11073-10101:2020)
Health informatics - Point-of-care medical device communication - Part 10101:
Nomenclature (ISO/IEEE FDIS 11073-10101:2020)
Medizinische Informatik - Kommunikation patientennaher medizinischer Geräte - Teil
10101: Nomenklatur (ISO/IEEE FDIS 11073-10101:2020)
Informatique de santé - Communication entre dispositifs médicaux sur le site des soins -
Partie 10101: Nomenclature (ISO/IEEE FDIS 11073-10101:2020)
Ta slovenski standard je istoveten z: prEN ISO 11073-10101
ICS:
01.040.35 Informacijska tehnologija. Information technology
(Slovarji) (Vocabularies)
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
oSIST prEN ISO 11073-10101:2020 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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oSIST prEN ISO 11073-10101:2020

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oSIST prEN ISO 11073-10101:2020
FINAL
INTERNATIONAL ISO/IEEE
DRAFT
STANDARD FDIS
11073-10101
ISO/TC 215
Health informatics — Device
Secretariat: ANSI
interoperability —
Voting begins on:
2020-01-02
Part 10101:
Voting terminates on:
Point-of-care medical device
2020-05-21
communication — Nomenclature
This document is circulated as received from the committee secretariat.
FAST TRACK PROCEDURE
ISO/CEN PARALLEL PROCESSING
RECIPIENTS OF THIS DRAFT ARE INVITED TO
SUBMIT, WITH THEIR COMMENTS, NOTIFICATION
OF ANY RELEVANT PATENT RIGHTS OF WHICH
THEY ARE AWARE AND TO PROVIDE SUPPOR TING
DOCUMENTATION.
IN ADDITION TO THEIR EVALUATION AS
Reference number
BEING ACCEPTABLE FOR INDUSTRIAL, TECHNO-
ISO/IEEE FDIS 11073-10101:2020(E)
LOGICAL, COMMERCIAL AND USER PURPOSES,
DRAFT INTERNATIONAL STANDARDS MAY ON
OCCASION HAVE TO BE CONSIDERED IN THE
LIGHT OF THEIR POTENTIAL TO BECOME STAN-
DARDS TO WHICH REFERENCE MAY BE MADE IN
©
NATIONAL REGULATIONS. IEEE 2019

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oSIST prEN ISO 11073-10101:2020
ISO/IEEE FDIS 11073-10101:2020(E)

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ii © IEEE 2019 – All rights reserved

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oSIST prEN ISO 11073-10101:2020
ISO/IEEE FDIS 11073-10101:2020(E)
Foreword
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ISO/IEEE 11073-10101 was prepared by the IEEE 11073 Standards Committee of the IEEE
Engineering in Medicine and Biology Society (as IEEE Std 11073-10101-2019) 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 second edition cancels and replaces the first edition (ISO/IEEE 11073-10101:2004), which has been
technically revised. It also incorporates the Amendment ISO/IEEE 11073-10101:2004/Amd 1:2017.
A list of all parts in the ISO/IEEE 11073 series can be found on the ISO website.
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© IEEE 2019 – All rights reserved iii

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oSIST prEN ISO 11073-10101:2020

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oSIST prEN ISO 11073-10101:2020
IEEE Std 11073-10101™-2019
(Revision of
ISO/IEEE 11073-10101:2004)
Health informatics—Point-of-care medical device communication
Part 10101: Nomenclature
Developed by the
IEEE 11073™ Standards Committee
of the
IEEE Engineering in Medicine and Biology Society
Approved 13 June 2019
IEEE SA Standards Board

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oSIST prEN ISO 11073-10101:2020
ISO/IEEE 11073-10101:2020(E)
Abstract: Within the context of the ISO/IEEE 11073 family of standards for point-of-care (POC)
and personal health devices (PHD) medical device communication (MDC), this standard provides
the nomenclature that supports both the domain information model and service model
components of the standards family, as well as the semantic content exchanged with medical
devices. The nomenclature is specialized for patient vital signs information representation and
medical device informatics, with major areas including concepts for electrocardiograph (ECG),
haemodynamics, respiration, blood gas, urine, fluid-related metrics, and neurology, as well as
specialized units of measurement, general device events, alarms, and body sites. The standard
defines both the architecture and major components of the nomenclature, along with extensive
definitions for each conceptual area.
Keywords: codes, IEEE 11073-10101™, IHE PCD-01, independent living, information model,
medical device communication, nomenclature, ontology, patient, personal health devices, PHD,
POC, point-of-care, semantics, service model, terminology

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SNOMED is a registered trademark of the College of American Pathologists (http://www.cap.org).
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of the publisher.
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oSIST prEN ISO 11073-10101:2020
ISO/IEEE 11073-10101:2020(E)
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oSIST prEN ISO 11073-10101:2020
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oSIST prEN ISO 11073-10101:2020
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5
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oSIST prEN ISO 11073-10101:2020
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Participants
At the time this draft standard was approved by the IEEE SA Standards Board, the Point-of-Care Devices
Working Group had the following membership:
Malcolm Clarke, Chair
Paul Schluter, Vice Chair

Spencer Crosswy Kai Hassing Mathieu Roullet
Steven Dain Stefan Karl Stefan Schlichting
Michael Faughn Brian Reinhold Richard Tayrien
Kenneth Fuchs Melvin Reynolds Michi Tietz
Marcus Garbe John Rhoads Jan Wittenber
John Garguilo Daidi Zhong

The following members of the individual balloting committee voted on this standard. Balloters may have
voted for approval, disapproval, or abstention.

Bjoern Andersen Noriyuki Ikeuchi Paul Schluter
Keith Chow Atsushi Ito Walter Struppler
Malcolm Clarke Stefan Karl Ganesh Subramanian
David Fuschi Piotr Karocki Lisa Ward
Randall Groves Martin Kasparick Jan Wittenber
Kai Hassing H. Moll Oren Yuen
Werner Hoelzl Beth Pumo Daidi Zhong
Stefan Schlichting

When the IEEE SA Standards Board approved this standard on 13 June 2019, it had the following
membership:

Gary Hoffman, Chair
Ted Burse, Vice Chair
Jean-Philippe Faure, Past Chair
Konstantinos Karachalios, Secretary

Masayuki Ariyoshi Thomas Koshy Annette D. Reilly
Ted Burse John D. Kulick Dorothy Stanley
Stephen D. Dukes David J. Law Sha Wei
J. Travis Griffith Joseph Levy Phil Wennblom
Guido Hiertz Howard Li Philip Winston
Christel Hunter Xiaohui Liu Howard Wolfman
Thomas Koshy Kevin Lu Feng Wu
Joseph L. Koepfinger* Daleep Mohla Jingyi Zhou
Andrew Myles

*Member Emeritus

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oSIST prEN ISO 11073-10101:2020
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Introduction
This introduction is not part of IEEE Std 11073-10101-2019, Health informatics—Point-of-Care Medical Device
Communication—Nomenclature.
ISO/IEEE 11073 standards enable communication between medical devices and external computer
systems. They provide automatic and detailed electronic data capture of patient vital signs information and
device operational data. The primary goals are to
⎯ Provide real-time plug-and-play interoperability for patient-connected medical devices.
⎯ Facilitate the efficient exchange of vital signs and medical device data, acquired at the point-of-
care, in all health care environments.
“Real-time” means that data from multiple devices can be retrieved, time correlated, and displayed or
processed in fractions of a second. “Plug-and-play” means that all the clinician has to do is make the
connection — the systems automatically detect, configure, and communicate without any other human
interaction.
“Efficient exchange of medical device data” means that information that is captured at the point-of-care
(e.g., patient vital signs data) can be archived, retrieved, and processed by many different types of
applications without extensive software and equipment support, and without needless loss of information.
The standards focus on acute care devices, such as patient monitors, ventilators, infusion pumps, ECG
devices, etc, and personal health devices and systems. They comprise a family of standards that can be
layered together to provide connectivity optimized for the specific devices being interfaced.
IEEE Std 11073-10101 was originally published in 2004 in conjunction with the International Organization
for Standardization (ISO). In 2015, IEEE published an amendment that expanded the nomenclature and
definitions covered in the standard to reflect the continued innovation in medical device and system design.
This 2019 revision integrates the amendment into the original text and further updates and expands the
nomenclature and definitions.
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oSIST prEN ISO 11073-10101:2020
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Contents
1. Scope . 20
2. Normative references . 20
3. Terms, definitions, symbols, and abbreviated terms. 22
3.1 Terms and definitions . 22
3.2 Symbols and abbreviated terms . 22
4. Conformance . 25
5. Introduction to the standard . 25
6. Application . 25
7. Semantics. 26
7.1 Attribution . 26
7.2 Coding . 27
7.2.1 Context-sensitivity . 27
7.2.2 Grouping . 28
7.3 Synonyms . 29
7.4 Deprecated terms . 29
7.5 Withdrawn terms . 29
8. Syntax . 29
8.1 Transfer . 29
8.1.1 Types . 29
8.1.2 Notation . 30
8.2 Programmatic form . 32
8.2.1 Attribution . 32
8.2.2 Notation . 32
9. Extensibility . 33
10. Version exporting . 33
Annex A (normative) Nomenclature semantics . 34
A.1 Overview of nomenclature for vital signs—Semantics . 34
A.2 Code assignment to the MDIB elements. 35
A.2.1 Overview . 35
A.2.2 Relationship to other standards . 35
A.2.3 Basic rules . 35
A.2.4 Coding spaces . 36
A.3 Data dictionary and codes for object-oriented modeling elements (Partition 1) . 45
A.3.1 Introduction . 45
A.3.2 Object-oriented modeling elements: inventory tables . 46
A.4 Data dictionary and codes for communication infrastructure (Partition 8) .
...

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