International ISO Standard >IEEE ISO/IEEE 11073-10472 Health informatics Device Second edition 2024-09 interoperability Part 10472: Personal health device communication Device specialization - Medication monitor Informatique de santé - Interoperabilité des dispositifs - Partie10472:Communicationentredispositifsdesante personnels-Spécialisation des dispositifs-Moniteur de surveillancedemedication Referencenumber ISO/IEEE11073-10472:2024(en) @IEEE2024 IS0/IEEE 11073-10472:2024(en) COPYRIGHT PROTECTED DOCUMENT @IEEE2024 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 3ParkAvenue, NewYork NY10016-5997,USA Email: [email protected] Website: www.ieee.org Published in Switzerland @ IEEE 2024- All rights reserved ii ISO/IEEE11073-10472:2024(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 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 i. 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 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. 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 ofthe date ofpublication ofthis document,Isohadnotreceivednotice 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 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 11073-10472 was prepared by the IEEE 11073 Standards Committee of the IEEE Engineering in Medicine and Biology Society (as IEEE Std 11073-1