Health informatics — Health cards — Numbering system and registration procedure for issuer identifiers

This document specifies a numbering system and registration procedure for identifying both healthcare application providers and health card holders in order to exchange information through the use of cards issued for healthcare services. This document focuses on the machine-readable cards of ID-1 type defined in ISO/IEC 7810 that are issued for healthcare services provided in a service area that crosses the national borders of two or more countries/areas. This document applies to healthcare data cards where the issuer and the application provider are the same party. This document applies directly, or refers, to existing International Standards for physical characteristics and recording techniques. Security issues follow the requirements of each healthcare data card system.

Informatique de santé — Cartes de santé — Système de numérotation et mode opératoire d'enregistrement pour les identificateurs d'émetteur

General Information

Status
Published
Publication Date
16-Jan-2022
Current Stage
5060 - Close of voting Proof returned by Secretariat
Completion Date
10-Dec-2021
Ref Project

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INTERNATIONAL ISO
STANDARD 20302
Third edition
2022-01
Health informatics — Health cards —
Numbering system and registration
procedure for issuer identifiers
Informatique de santé — Cartes de santé — Système de numérotation
et mode opératoire d'enregistrement pour les identificateurs
d'émetteur
Reference number
ISO 20302:2022(E)
© ISO 2022
---------------------- Page: 1 ----------------------
ISO 20302:2022(E)
COPYRIGHT PROTECTED DOCUMENT
© ISO 2022

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 either ISO at the address below

or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
© ISO 2022 – All rights reserved
---------------------- Page: 2 ----------------------
ISO 20302:2022(E)
Contents Page

Foreword ........................................................................................................................................................................................................................................iv

Introduction .................................................................................................................................................................................................................................v

1 Scope ................................................................................................................................................................................................................................. 1

2 Normative references ..................................................................................................................................................................................... 1

3 Terms and definitions .................................................................................................................................................................................... 1

4 Abbreviations .......................................................................................................................................................................................................... 2

5 Identifiers of the healthcare application providers ....................................................................................................... 2

5.1 General ........................................................................................................................................................................................................... 2

5.2 Structure of IIN ...................................................................................................................................................................................... 2

5.3 Structure of RID .................................................................................................................................................................................... 3

Annex A (normative) Structure of RID ..............................................................................................................................................................4

Bibliography ................................................................................................................................................................................................................................ 6

iii
© ISO 2022 – All rights reserved
---------------------- Page: 3 ----------------------
ISO 20302:2022(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. This document was drafted in accordance with the

editorial rules of the ISO/IEC Directives, Part 2 (see www.iso.org/directives).

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.

This document was prepared by Technical Committee ISO/TC 215, Health informatics.

This third edition cancels and replaces the second edition (ISO 20302:2014), which has been technically

revised.
The main changes compared to the previous edition are as follows:

— update of the description of IIN for consistency with the latest edition of ISO/IEC 7812-1 and

ISO/IEC 7812-2.

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.
© ISO 2022 – All rights reserved
---------------------- Page: 4 ----------------------
ISO 20302:2022(E)
Introduction

This document describes a numbering system and registration procedure for issuing identifiers of

machine-readable cards used in the field of healthcare.

The purpose of using machine-readable cards in the field of healthcare is to improve the quality

of the health service and increase the efficient use of healthcare resources in the field. The primary

consideration in creating this document has been to improve patient service and patient safety, as well

as improve the practical use of healthcare data cards in clinical fields.
a) The following are outside the scope of this document:
— standardizing the clinical practice of medicine,
— defining a standardized healthcare delivery service structure,

— the characteristics and operation of other cards, which are not covered by this document.

In past years, healthcare data cards have been used to exchange healthcare data by placing necessary

and appropriate information on the surface of the cards in order to implement the health service of each

country. However, as people now move more frequently across borders, healthcare data cards issued in

one country or area are increasingly being used in another and, with this consideration in mind, this

document has been designed to apply to healthcare data cards that will be used internationally.

b) This document is applicable to healthcare data cards used for healthcare services provided by the

card issuer.

c) The numbering system and registration procedure is technology independent and designed to fit

relevant technologies and recording techniques for healthcare data cards.

The data elements and data structures in healthcare data cards are standardized in ISO 21549 (all parts).

© ISO 2022 – All rights reserved
---------------------- Page: 5 ----------------------
INTERNATIONAL STANDARD ISO 20302:2022(E)
Health informatics — Health cards — Numbering system
and registration procedure for issuer identifiers
1 Scope

This document specifies a numbering system and registration procedure for identifying both healthcare

application providers and health card holders in order to exchange information through the use of cards

issued for healthcare services.
This document focuses on the machine-readable card
...

FINAL
INTERNATIONAL ISO/FDIS
DRAFT
STANDARD 20302
ISO/TC 215
Health informatics — Health cards —
Secretariat: ANSI
Numbering system and registration
Voting begins on:
2021-10-14 procedure for issuer identifiers
Voting terminates on:
Informatique de santé — Cartes de santé — Système de numérotation
2021-12-09
et mode opératoire d'enregistrement pour les identificateurs
d'émetteur
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/FDIS 20302:2021(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. © ISO 2021
---------------------- Page: 1 ----------------------
ISO/FDIS 20302:2021(E)
COPYRIGHT PROTECTED DOCUMENT
© ISO 2021

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 either ISO at the address below

or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
© ISO 2021 – All rights reserved
---------------------- Page: 2 ----------------------
ISO/FDIS 20302:2021(E)
Contents Page

Foreword ........................................................................................................................................................................................................................................iv

Introduction .................................................................................................................................................................................................................................v

1 Scope ................................................................................................................................................................................................................................. 1

2 Normative references ..................................................................................................................................................................................... 1

3 Terms and definitions .................................................................................................................................................................................... 1

4 Abbreviations .......................................................................................................................................................................................................... 2

5 Identifiers of the healthcare application providers ....................................................................................................... 2

5.1 General ........................................................................................................................................................................................................... 2

5.2 Structure of IIN ...................................................................................................................................................................................... 2

5.3 Structure of RID .................................................................................................................................................................................... 3

Annex A (normative) Structure of RID ..............................................................................................................................................................4

Bibliography ................................................................................................................................................................................................................................ 6

iii
© ISO 2021 – All rights reserved
---------------------- Page: 3 ----------------------
ISO/FDIS 20302:2021(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. This document was drafted in accordance with the

editorial rules of the ISO/IEC Directives, Part 2 (see www.iso.org/directives).

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.

This document was prepared by Technical Committee ISO/TC 215, Health informatics.

This third edition cancels and replaces the second edition (ISO 20302:2014), which has been technically

revised.
The main changes compared to the previous edition are as follows:

— update of the description of IIN for consistency with the latest edition of ISO/IEC 7812-1 and ISO/

IEC 7812-2.

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.
© ISO 2021 – All rights reserved
---------------------- Page: 4 ----------------------
ISO/FDIS 20302:2021(E)
Introduction

This document describes a numbering system and registration procedure for issuing identifiers of

machine-readable cards used in the field of healthcare.

The purpose of using machine-readable cards in the field of healthcare is to improve the quality

of the health service and increase the efficient use of healthcare resources in the field. The primary

consideration in creating this document has been to improve patient service and patient safety, as well

as improve the practical use of healthcare data cards in clinical fields.
a) The following are outside the scope of this document:
— standardizing the clinical practice of medicine,
— defining a standardized healthcare delivery service structure,

— the characteristics and operation of other cards, which are not covered by this document.

In past years, healthcare data cards have been used to exchange healthcare data by placing necessary

and appropriate information on the surface of the cards in order to implement the health service of each

country. However, as people now move more frequently across borders, healthcare data cards issued in

one country or area are increasingly being used in another and, with this consideration in mind, this

document has been designed to apply to healthcare data cards that will be used internationally.

b) This document is applicable to healthcare data cards used for healthcare services provided by the

card issuer.

c) The numbering system and registration procedure is technology independent and designed to fit

relevant technologies and recording techniques for healthcare data cards.

The data elements and data structures in healthcare data cards are standardized in ISO 21549 (all

parts).
© ISO 2021 – All rights reserved
---------------------- Page: 5 ----------------------
FINAL DRAFT INTERNATIONAL STANDARD ISO/FDIS 20302:2021(E)
Health informatics — Health cards — Numbering system
and registration procedure for issuer identifiers
1 S
...

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