SIST EN ISO 11073-10101:2021
(Main)Health informatics - Device interoperability - Part 10101:Point-of-care medical device communication - Nomenclature (ISO/IEEE 11073-10101:2020)
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
Relations
Standards Content (Sample)
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
---------------------- Page: 2 ----------------------
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.
---------------------- Page: 3 ----------------------
SIST EN ISO 11073-10101:2021
EN ISO 11073-10101:2020 (E)
Contents Page
European foreword . 3
2
---------------------- Page: 4 ----------------------
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
---------------------- Page: 5 ----------------------
SIST EN ISO 11073-10101:2021
---------------------- Page: 6 ----------------------
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
---------------------- Page: 7 ----------------------
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
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from IEEE at the address below.
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
---------------------- Page: 8 ----------------------
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
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.
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
ISO list of patent declarations received (see www.iso.org/patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the World
Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT), see www.iso.org/
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
---------------------- Page: 9 ----------------------
SIST EN ISO 11073-10101:2021
---------------------- Page: 10 ----------------------
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
•
The Institute of Electrical and Electronics Engineers, Inc.
3 Park Avenue, New York, NY 10016-5997, USA
Copyright © 2019 by The Institute of Electrical and Electronics Engineers, Inc.
All rights reserved. Published 9 October 2019. Printed in the United States of America.
IEEE is a registered trademark in the U.S. Patent & Trademark Office, owned by The Institute of Electrical and Electronics Engineers,
Incorporated.
HL7 is a registered trademark of Health Level Seven, Inc. (http://www.hl7.org).
SNOMED is a registered trademark of the College of American Pathologists (http://www.cap.org).
PDF: ISBN 978-1-5044-5981-5 STD23760
Print: ISBN 978-1-5044-5982-2 STDPD23760
IEEE prohibits discrimination, harassment, and bullying.
For more information, visit http://www.ieee.org/web/aboutus/whatis/policies/p9-26.html.
No part of this publication may be reproduced in any form, in an electronic retrieval system or otherwise, without the prior written permission
of the publisher.
2
Copyright © 2018 IEEE. All rights reserved.
---------------------- Page: 12 ----------------------
SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)
Important Notices and Disclaimers Concerning IEEE Standards Documents
IEEE documents are made available for use subject to important notices and legal disclaimers. These
notices and disclaimers, or a reference to this page, appear in all standards and may be found under the
heading “Important Notices and Disclaimers Concerning IEEE Standards Documents.” They can also be
obtained on request from IEEE or viewed at http://standards.ieee.org/ipr/disclaimers.html.
Notice and Disclaimer of Liability Concerning the Use of IEEE Standards
Documents
IEEE Standards documents (standards, recommended practices, and guides), both full-use and trial-use, are
developed within IEEE Societies and the Standards Coordinating Committees of the IEEE Standards
Association (“IEEE SA”) Standards Board. IEEE (“the Institute”) develops its standards through a
consensus development process, approved by the American National Standards Institute (“ANSI”), which
brings together volunteers representing varied viewpoints and interests to achieve the final product. IEEE
Standards are documents developed through scientific, academic, and industry-based technical working
groups. Volunteers in IEEE working groups are not necessarily members of the Institute and participate
without compensation from IEEE. While IEEE administers the process and establishes rules to promote
fairness in the consensus development process, IEEE does not independently evaluate, test, or verify the
accuracy of any of the information or the soundness of any judgments contained in its standards.
IEEE Standards do not guarantee or ensure safety, security, health, or environmental protection, or ensure
against interference with or from other devices or networks. Implementers and users of IEEE Standards
documents are responsible for determining and complying with all appropriate safety, security,
environmental, health, and interference protection practices and all applicable laws and regulations.
IEEE does not warrant or represent the accuracy or content of the material contained in its standards, and
expressly disclaims all warranties (express, implied and statutory) not included in this or any other
document relating to the standard, including, but not limited to, the warranties of: merchantability; fitness
for a particular purpose; non-infringement; and quality, accuracy, effectiveness, currency, or completeness
of material. In addition, IEEE disclaims any and all conditions relating to: results; and workmanlike effort.
IEEE standards documents are supplied “AS IS” and “WITH ALL FAULTS.”
Use of an IEEE standard is wholly voluntary. The existence of an IEEE standard does not imply that there
are no other ways to produce, test, measure, purchase, market, or provide other goods and services related
to the scope of the IEEE standard. Furthermore, the viewpoint expressed at the time a standard is approved
and issued is subject to change brought about through developments in the state of the art and comments
received from users of the standard.
In publishing and making its standards available, IEEE is not suggesting or rendering professional or other
services for, or on behalf of, any person or entity nor is IEEE undertaking to perform any duty owed by any
other person or entity to another. Any person utilizing any IEEE Standards document, should rely upon his
or her own independent judgment in the exercise of reasonable care in any given circumstances or, as
appropriate, seek the advice of a competent professional in determining the appropriateness of a given
IEEE standard.
IN NO EVENT SHALL IEEE BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL,
EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT LIMITED TO:
PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE, DATA, OR PROFITS;
OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY THEORY OF LIABILITY,
WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT (INCLUDING NEGLIGENCE OR
OTHERWISE) ARISING IN ANY WAY OUT OF THE PUBLICATION, USE OF, OR RELIANCE
UPON ANY STANDARD, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE AND
REGARDLESS OF WHETHER SUCH DAMAGE WAS FORESEEABLE.
3
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 13 ----------------------
SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)
Translations
The IEEE consensus development process involves the review of documents in English only. In the event
that an IEEE standard is translated, only the English version published by IEEE should be considered the
approved IEEE standard.
Official statements
A statement, written or oral, that is not processed in accordance with the IEEE SA Standards Board
Operations Manual shall not be considered or inferred to be the official position of IEEE or any of its
committees and shall not be considered to be, or be relied upon as, a formal position of IEEE. At lectures,
symposia, seminars, or educational courses, an individual presenting information on IEEE standards shall
make it clear that his or her views should be considered the personal views of that individual rather than the
formal position of IEEE.
Comments on standards
Comments for revision of IEEE Standards documents are welcome from any interested party, regardless of
membership affiliation with IEEE. However, IEEE does not provide consulting information or advice
pertaining to IEEE Standards documents. Suggestions for changes in documents should be in the form of a
proposed change of text, together with appropriate supporting comments. Since IEEE standards represent a
consensus of concerned interests, it is important that any responses to comments and questions also receive
the concurrence of a balance of interests. For this reason, IEEE and the members of its societies and
Standards Coordinating Committees are not able to provide an instant response to comments or questions
except in those cases where the matter has previously been addressed. For the same reason, IEEE does not
respond to interpretation requests. Any person who would like to participate in revisions to an IEEE
standard is welcome to join the relevant IEEE working group.
Comments on standards should be submitted to the following address:
Secretary, IEEE SA Standards Board
445 Hoes Lane
Piscataway, NJ 08854 USA
Laws and regulations
Users of IEEE Standards documents should consult all applicable laws and regulations. Compliance with
the provisions of any IEEE Standards document does not imply compliance to any applicable regulatory
requirements. Implementers of the standard are responsible for observing or referring to the applicable
regulatory requirements. IEEE does not, by the publication of its standards, intend to urge action that is not
in compliance with applicable laws, and these documents may not be construed as doing so.
Copyrights
IEEE draft and approved standards are copyrighted by IEEE under U.S. and international copyright laws.
They are made available by IEEE and are adopted for a wide variety of both public and private uses. These
include both use, by reference, in laws and regulations, and use in private self-regulation, standardization,
and the promotion of engineering practices and methods. By making these documents available for use and
adoption by public authorities and private users, IEEE does not waive any rights in copyright to the
documents.
4
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 14 ----------------------
SIST EN ISO 11073-10101:2021
ISO/IEEE 11073-10101:2020(E)
Photocopies
Subject to payment of the appropriate fee, IEEE will grant users a limited, non-exclusive license to
photocopy portions of any individual standard for company or organizational internal use or individual,
non-commercial use only. To arrange for payment of licensing fees, please contact Copyright Clearance
Center, Customer Service, 222 Rosewood Drive, Danvers, MA 01923 USA; +1 978 750 8400. Permission
to photocopy portions of any individual standard for educational classroom use can also be obtained
through the Copyright Clearance Center.
Updating of IEEE Standards documents
Users of IEEE Standards documents should be aware that these documents may be superseded at any time
by the issuance of new editions or may be amended from time to time through the issuance of amendments,
corrigenda, or errata. A current IEEE document at any point in time consists of the current edition of the
document together with any amendments, corrigenda, or errata then in effect.
Every IEEE standard is subjected to review at least every ten years. When a document is more than ten
years old and has not undergone a revision process, it is reasonable to conclude that its contents, although
still of some value, do not wholly reflect the present state of the art. Users are cautioned to check to
determine that they have the latest edition of any IEEE standard.
In order to determine whether a given document is the current edition and whether it has been amended
through the issuance of amendments, corrigenda, or errata, visit the IEEE Xplore at
http://ieeexplore.ieee.org/ or contact IEEE at the address listed previously. For more information about the
IEEE SA or IEEE’s standards development process, visit the IEEE SA Website at http://standards.ieee.org.
Errata
Errata, if any, for all IEEE standards can be accessed on the IEEE SA Website at the following URL:
http://standards.ieee.org/findstds/errata/index.html. Users are encouraged to check this URL for errata
periodically.
Patents
Attention is called to the possibility that implementation of this standard may require use of subject matter
covered by patent rights. By publication of this standard, no position is taken by the IEEE with respect to
the existence or validity of any patent rights in connection therewith. If a patent holder or patent applicant
has filed a statement of assurance via an Accepted Letter of Assurance, then the statement is listed on the
IEEE SA Website at http://standards.ieee.org/about/sasb/patcom/patents.html. Letters of Assurance may
indicate whether the Submitter is willing or unwilling to grant licenses under patent rights without
compensation or under reasonable rates, with reasonable terms and conditions that are demonstrably free of
any unfair discrimination to applicants desiring to obtain such licenses.
Essential Patent Claims may exist for which a Letter of Assurance has not been received. The IEEE is not
responsible for identifying Essential Patent Claims for which a license may be required, for conducting
inquiries into the legal validity or scope of Patents Claims, or determining whether any licensing terms or
conditions provided in connection with submission of a Letter of Assurance, 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 the IEEE Standards Association.
5
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 15 ----------------------
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
6
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 16 ----------------------
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.
7
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 17 ----------------------
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.
---------------------- Page: 1 ----------------------
oSIST prEN ISO 11073-10101:2020
---------------------- Page: 2 ----------------------
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
---------------------- Page: 3 ----------------------
oSIST prEN ISO 11073-10101:2020
ISO/IEEE FDIS 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
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from IEEE at the address below.
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
---------------------- Page: 4 ----------------------
oSIST prEN ISO 11073-10101:2020
ISO/IEEE FDIS 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
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.
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
ISO list of patent declarations received (see www.iso.org/patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the World
Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT), see www.iso.org/
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
---------------------- Page: 5 ----------------------
oSIST prEN ISO 11073-10101:2020
---------------------- Page: 6 ----------------------
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
---------------------- Page: 7 ----------------------
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
•
The Institute of Electrical and Electronics Engineers, Inc.
3 Park Avenue, New York, NY 10016-5997, USA
Copyright © 2019 by The Institute of Electrical and Electronics Engineers, Inc.
All rights reserved. Published 9 October 2019. Printed in the United States of America.
IEEE is a registered trademark in the U.S. Patent & Trademark Office, owned by The Institute of Electrical and Electronics Engineers,
Incorporated.
HL7 is a registered trademark of Health Level Seven, Inc. (http://www.hl7.org).
SNOMED is a registered trademark of the College of American Pathologists (http://www.cap.org).
PDF: ISBN 978-1-5044-5981-5 STD23760
Print: ISBN 978-1-5044-5982-2 STDPD23760
IEEE prohibits discrimination, harassment, and bullying.
For more information, visit http://www.ieee.org/web/aboutus/whatis/policies/p9-26.html.
No part of this publication may be reproduced in any form, in an electronic retrieval system or otherwise, without the prior written permission
of the publisher.
2
Copyright © 2018 IEEE. All rights reserved.
---------------------- Page: 8 ----------------------
oSIST prEN ISO 11073-10101:2020
ISO/IEEE 11073-10101:2020(E)
Important Notices and Disclaimers Concerning IEEE Standards Documents
IEEE documents are made available for use subject to important notices and legal disclaimers. These
notices and disclaimers, or a reference to this page, appear in all standards and may be found under the
heading “Important Notices and Disclaimers Concerning IEEE Standards Documents.” They can also be
obtained on request from IEEE or viewed at http://standards.ieee.org/ipr/disclaimers.html.
Notice and Disclaimer of Liability Concerning the Use of IEEE Standards
Documents
IEEE Standards documents (standards, recommended practices, and guides), both full-use and trial-use, are
developed within IEEE Societies and the Standards Coordinating Committees of the IEEE Standards
Association (“IEEE SA”) Standards Board. IEEE (“the Institute”) develops its standards through a
consensus development process, approved by the American National Standards Institute (“ANSI”), which
brings together volunteers representing varied viewpoints and interests to achieve the final product. IEEE
Standards are documents developed through scientific, academic, and industry-based technical working
groups. Volunteers in IEEE working groups are not necessarily members of the Institute and participate
without compensation from IEEE. While IEEE administers the process and establishes rules to promote
fairness in the consensus development process, IEEE does not independently evaluate, test, or verify the
accuracy of any of the information or the soundness of any judgments contained in its standards.
IEEE Standards do not guarantee or ensure safety, security, health, or environmental protection, or ensure
against interference with or from other devices or networks. Implementers and users of IEEE Standards
documents are responsible for determining and complying with all appropriate safety, security,
environmental, health, and interference protection practices and all applicable laws and regulations.
IEEE does not warrant or represent the accuracy or content of the material contained in its standards, and
expressly disclaims all warranties (express, implied and statutory) not included in this or any other
document relating to the standard, including, but not limited to, the warranties of: merchantability; fitness
for a particular purpose; non-infringement; and quality, accuracy, effectiveness, currency, or completeness
of material. In addition, IEEE disclaims any and all conditions relating to: results; and workmanlike effort.
IEEE standards documents are supplied “AS IS” and “WITH ALL FAULTS.”
Use of an IEEE standard is wholly voluntary. The existence of an IEEE standard does not imply that there
are no other ways to produce, test, measure, purchase, market, or provide other goods and services related
to the scope of the IEEE standard. Furthermore, the viewpoint expressed at the time a standard is approved
and issued is subject to change brought about through developments in the state of the art and comments
received from users of the standard.
In publishing and making its standards available, IEEE is not suggesting or rendering professional or other
services for, or on behalf of, any person or entity nor is IEEE undertaking to perform any duty owed by any
other person or entity to another. Any person utilizing any IEEE Standards document, should rely upon his
or her own independent judgment in the exercise of reasonable care in any given circumstances or, as
appropriate, seek the advice of a competent professional in determining the appropriateness of a given
IEEE standard.
IN NO EVENT SHALL IEEE BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL,
EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT LIMITED TO:
PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE, DATA, OR PROFITS;
OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY THEORY OF LIABILITY,
WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT (INCLUDING NEGLIGENCE OR
OTHERWISE) ARISING IN ANY WAY OUT OF THE PUBLICATION, USE OF, OR RELIANCE
UPON ANY STANDARD, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE AND
REGARDLESS OF WHETHER SUCH DAMAGE WAS FORESEEABLE.
3
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 9 ----------------------
oSIST prEN ISO 11073-10101:2020
ISO/IEEE 11073-10101:2020(E)
Translations
The IEEE consensus development process involves the review of documents in English only. In the event
that an IEEE standard is translated, only the English version published by IEEE should be considered the
approved IEEE standard.
Official statements
A statement, written or oral, that is not processed in accordance with the IEEE SA Standards Board
Operations Manual shall not be considered or inferred to be the official position of IEEE or any of its
committees and shall not be considered to be, or be relied upon as, a formal position of IEEE. At lectures,
symposia, seminars, or educational courses, an individual presenting information on IEEE standards shall
make it clear that his or her views should be considered the personal views of that individual rather than the
formal position of IEEE.
Comments on standards
Comments for revision of IEEE Standards documents are welcome from any interested party, regardless of
membership affiliation with IEEE. However, IEEE does not provide consulting information or advice
pertaining to IEEE Standards documents. Suggestions for changes in documents should be in the form of a
proposed change of text, together with appropriate supporting comments. Since IEEE standards represent a
consensus of concerned interests, it is important that any responses to comments and questions also receive
the concurrence of a balance of interests. For this reason, IEEE and the members of its societies and
Standards Coordinating Committees are not able to provide an instant response to comments or questions
except in those cases where the matter has previously been addressed. For the same reason, IEEE does not
respond to interpretation requests. Any person who would like to participate in revisions to an IEEE
standard is welcome to join the relevant IEEE working group.
Comments on standards should be submitted to the following address:
Secretary, IEEE SA Standards Board
445 Hoes Lane
Piscataway, NJ 08854 USA
Laws and regulations
Users of IEEE Standards documents should consult all applicable laws and regulations. Compliance with
the provisions of any IEEE Standards document does not imply compliance to any applicable regulatory
requirements. Implementers of the standard are responsible for observing or referring to the applicable
regulatory requirements. IEEE does not, by the publication of its standards, intend to urge action that is not
in compliance with applicable laws, and these documents may not be construed as doing so.
Copyrights
IEEE draft and approved standards are copyrighted by IEEE under U.S. and international copyright laws.
They are made available by IEEE and are adopted for a wide variety of both public and private uses. These
include both use, by reference, in laws and regulations, and use in private self-regulation, standardization,
and the promotion of engineering practices and methods. By making these documents available for use and
adoption by public authorities and private users, IEEE does not waive any rights in copyright to the
documents.
4
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 10 ----------------------
oSIST prEN ISO 11073-10101:2020
ISO/IEEE 11073-10101:2020(E)
Photocopies
Subject to payment of the appropriate fee, IEEE will grant users a limited, non-exclusive license to
photocopy portions of any individual standard for company or organizational internal use or individual,
non-commercial use only. To arrange for payment of licensing fees, please contact Copyright Clearance
Center, Customer Service, 222 Rosewood Drive, Danvers, MA 01923 USA; +1 978 750 8400. Permission
to photocopy portions of any individual standard for educational classroom use can also be obtained
through the Copyright Clearance Center.
Updating of IEEE Standards documents
Users of IEEE Standards documents should be aware that these documents may be superseded at any time
by the issuance of new editions or may be amended from time to time through the issuance of amendments,
corrigenda, or errata. A current IEEE document at any point in time consists of the current edition of the
document together with any amendments, corrigenda, or errata then in effect.
Every IEEE standard is subjected to review at least every ten years. When a document is more than ten
years old and has not undergone a revision process, it is reasonable to conclude that its contents, although
still of some value, do not wholly reflect the present state of the art. Users are cautioned to check to
determine that they have the latest edition of any IEEE standard.
In order to determine whether a given document is the current edition and whether it has been amended
through the issuance of amendments, corrigenda, or errata, visit the IEEE Xplore at
http://ieeexplore.ieee.org/ or contact IEEE at the address listed previously. For more information about the
IEEE SA or IEEE’s standards development process, visit the IEEE SA Website at http://standards.ieee.org.
Errata
Errata, if any, for all IEEE standards can be accessed on the IEEE SA Website at the following URL:
http://standards.ieee.org/findstds/errata/index.html. Users are encouraged to check this URL for errata
periodically.
Patents
Attention is called to the possibility that implementation of this standard may require use of subject matter
covered by patent rights. By publication of this standard, no position is taken by the IEEE with respect to
the existence or validity of any patent rights in connection therewith. If a patent holder or patent applicant
has filed a statement of assurance via an Accepted Letter of Assurance, then the statement is listed on the
IEEE SA Website at http://standards.ieee.org/about/sasb/patcom/patents.html. Letters of Assurance may
indicate whether the Submitter is willing or unwilling to grant licenses under patent rights without
compensation or under reasonable rates, with reasonable terms and conditions that are demonstrably free of
any unfair discrimination to applicants desiring to obtain such licenses.
Essential Patent Claims may exist for which a Letter of Assurance has not been received. The IEEE is not
responsible for identifying Essential Patent Claims for which a license may be required, for conducting
inquiries into the legal validity or scope of Patents Claims, or determining whether any licensing terms or
conditions provided in connection with submission of a Letter of Assurance, 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 the IEEE Standards Association.
5
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 11 ----------------------
oSIST prEN ISO 11073-10101:2020
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
6
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 12 ----------------------
oSIST prEN ISO 11073-10101:2020
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.
7
Copyright © 2019 IEEE. All rights reserved.
---------------------- Page: 13 ----------------------
oSIST prEN ISO 11073-10101:2020
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 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) .
...
Questions, Comments and Discussion
Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.