International ISO Standard >IEEE ISO/IEEE 11073-10701 First edition Health informatics Device 2024-09 interoperability - Part 10701: Point-of-care medical device communication Metric provisioning by participants in a Service-oriented Device Connectivity (SDC) system Informatiquedesante-Interoperabilitedesdispositifs Partie10701:Communication entre dispositifs medicaux surle sitede soins-Fourniture de metriquespar les participants un systeme de connectivite des dispositifs orientee services (SDC) Reference number IS0/IEEE11073-10701:2024(en) COPYRIGHTPROTECTEDDOCUMENT @IEEE2024 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 IS0/IEEE11073-10701:2024(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 whicha technical 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 thework.Iso collaborates closely withtheInternational Electrotechnical Commission (IEC) on all matters ofelectrotechnical standardization. Theprocedures used to develop this documentand 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 StandardsAssociation (IEEE-SA) StandardsBoard.The IEEEdevelops 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 necessarilymembers of the Institute and serve without compensation.Whilethe IEEE administers theprocess and establishes rules to promote fairness in the consensus developmentprocess,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 takesnoposition concerning the evidence,validity or applicability ofany 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 implementthis document.However, implementers are cautioned that this may not represent the latest information, whichmay beobtained 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 constitutean endorsement. For an explanation of the voluntary nature of standards, themeaning of Iso specific terms and expressions related to conformity assessment,as well asinformation about Iso's adherence tothe WorldTrade Organization (WTO) principles in the Technical Barriers to Trade (TBT), see www.iso.org/iso/foreword.html. IS0/IEEE11073-10701waspreparedbytheIEEE11073StandardsCommitteeoftheIEEEEngineeringin Medicine and Biology Society (as IEEE Std 11073-10701) and drafted in accordance with its editorial rules. It cooperationagreementbetweenISOandIEEE,byTechnicalCommitteeISO/TC215,Healthinform