ISO/IEEE INTERNATIONAL STANDARD 11073-10207 First edition 2019-03 Health informatics Personal health device communication - Part 10207: Domain information and service model for service-oriented point-of- care medical device communication Informatique de santé - Communication entre dispositifs de sante personnels Partie 10207: Informations de domaine et modele de services pour la communication orientee services entre dispositifs medicaux sur le site des soins ISO Reference number IS0/IEEE11073-10207:2019(E) IEEE @IEEE2018 IS0/IEEE11073-10207:2019(E) COPYRIGHTPROTECTEDDOCUMENT IEEE2018 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 theinternetor anintranet,withoutprior writtenpermission.Permission canberequestedfromIEEEattheaddressbelow. InstituteofElectricalandElectronicsEngineers,Inc 3 Park Avenue, New York NY 10016-5997,USA Email: [email protected] Website:www.ieee.org Published in Switzerland ii @ IEEE 2018 -All rights reserved IS0/IEEE 11073-10207:2019(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 (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 thefinalproduct.VolunteersarenotnecessarilymembersoftheInstituteandservewithout 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 IS0/IEEE11073-10207 was prepared by the IEEE11073 Standards Committee of the IEEE Engineering in Medicine and Biology Society (as IEEE Std 11073-10207-2017) 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 Com