ISO/IEEE INTERNATIONAL STANDARD 11073-10417 Third edition 2017-04 Health informatics Personal health device communication Part 10417: Device specialization Glucose meter Informatique de santé-Communication entre dispositifs medicaux sur le site dessoins- Partie 10417: Spécialisation des dispositifs -Glucometre Reference number [so IS0/IEEE11073-10417:2017(E) >IEEE @IEEE2015 International Organization for Standardization nSeeZHEJIANG INST OF STANDARDIZATION C1 5956617 IS0/IEEE11073-10417:2017(E) COPYRIGHTPROTECTEDDOCUMENT @IEEE2015 All rights reserved. Unless otherwise specified, 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.PermissioncanberequestedfromeitherIsOorIEEEattheaddressbeloworIso'smemberbodyinthecountryof the requester. ISO copyright office InstituteofElectricalandElectronicsEngineers,Inc Ch. de Blandonnet 8. CP 401 3 Park Avenue, New York CH-1214 Vernier, Geneva, Switzerland NY 10016-5997,USA Tel. +41 22 749 01 11 Fax +4122749 09 47 [email protected] [email protected] www.iso.org www.ieee.org Luicensee-ZHEJANG INSTOF STANDARDIZATIddFEEe2Q15 - All rights reserved ted without license from IHS Not for Resale, 2017/6/28 01:05:0 IS0/IEEE 11073-10417:2017(E) Foreword Iso(theInternationalOrganizationforStandardization)isaworldwidefederationofnationalstandardsbodies (Iso member bodies). The work of preparing International Standards is normally carried out through ISO technicalcommittees.Eachmemberbodyinterestedinasubjectforwhichatechnicalcommitteehasbeen 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. 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 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. The main task of technical committees is to prepare International Standards. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publication as an InternationalStandardrequiresapprovalbyatleast75%ofthememberbodiescastingavote. Attention is called to the possibility that implementation of this standard may require the use of subject matter coveredbypatentrights.Bypublicationofthisstandard,nopositionistakenwithrespecttotheexistenceor validity of any patent rights in connection therewith. Iso/IEEE is not responsible for identifying essential patents or patent claims for which a license may be required, for conducting inquiries into the legal validity or scope of patents or patent claims or determining whether any licensing terms or conditions provided in connection with submission of a Letter of Assurance or a Patent Statement and Licensing Declaration Form, if any or in any licensing agreements are reasonable or non-discriminatory. Users of this standard are expressly advised that determination of the validity of any patent rights, and the risk of infringement of such rights, is entirely their own responsibility. Further information may be obtained from ISO or the IEEE Standards Association IS0/IEEE 11073-10417 was prepared by the 11073 Committee of the Engineering in Medicine and Biology Health informatics, in parallel with its approval by the Iso member bodies, under the “fast-track procedure' defined in the Partner Standards Dev