International ISO Standard >IEEE ISO/IEEE 11073-10206 First edition HealthinformaticsDevice interoperability - 2024-07 Part 10206: Personal health device communication Abstract content information model Informatique de sante-Interoperabilite des dispositifs- Partie10206:Communication entredispositifsde sante personnels-Modeled'information decontenuabstrait Referencenumber IS0/IEEE11073-10206:2024(en) ?IEEE2023 IS0/IEEE11073-10206:2024(en) COPYRIGHTPROTECTEDDOCUMENT @IEEE2023 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 NY10016-5997,USA Email: stds.ipr@ieee.org Website: www.ieee.org Published in Switzerland @ IEEE 2023 -Allrights reserved ii IS0/IEEE11073-10206:2024(en) 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 atechnical committee has been established has the right tobe 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 document 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 bringstogether volunteersrepresentingvariedviewpoints andintereststo achievethefinal product Volunteers are not necessarily members of the Institute and serve without compensation.While the IEEE administerstheprocessandestablishesrulestopromotefairnessintheconsensusdevelopmentprocess,the IEEE does not independently evaluate, test, or verify the accuracy of any of the information contained in its standards. Iso draws attention to the possibility that the implementation of this document may involve the use of (a) patent(s). IsO takes no position concerning the evidence, validity or applicability of any claimed patent rights in respect thereof. As of the date of publication of this document, Iso had not received notice of (a) patent(s) which may be required to implement this document. However, implementers are cautioned that this may not represent the latest information, which may be obtained from the patent database available at www.iso.org/patents. IsO shall not be held responsible for identifying any or all such patent rights. 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. IS0/IEEE11073-10206waspreparedbytheIEEE11073StandardsCommittee of theIEEEEngineering in Medicine and Biology Society (as IEEE Std 11073-10206-2022) and drafted in accordance with its editorial rules. It was adopted, under the "fast-track procedure" defined in the Partner Standards Development Organization c