ISO/IEEE INTERNATIONAL STANDARD 11073-20601 Third edition 2022-12 Health informatics Device interoperability - Part 20601: Personal health device communication - Application profile Optimized exchange protocol Informatique de santé - Interopérabilite des dispositifs - Partie 20601: Communication entre dispositifs de santé personnels - Profil d'application - Protocole d'echange optimisé rso Reference number IS0/IEEE11073-20601:2022(E) IEEE @IEEE2019 IS0/IEEE 11073-20601:2022(E) COPYRIGHTPROTECTEDDOCUMENT IEEE2019 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 3ParkAvenue,NewYork NY10016-5997,USA Email: [email protected] Website: www.ieee.org Published in Switzerland ii @ IEEE 2019 - All rights reserved IS0/IEEE 11073-20601:2022(E) wx:ivd-by Foreword Iso (the International Organization for Standardization) is a worldwide federation of national standards bodies (so 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 constituteanendorsement. 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. IS0/IEEE 11073-20601 was prepared by the IEEE 11073 Standards Committee of the IEEE Engineering in Medicine and Biology Society (as IEEE Std 11073-20601-2019) 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 third edition cancels and replaces the second edition (IS0/IEEE 11073-20601:2016), whi