INTERNATIONAL ISO/IEEE STANDARD 11073-10422 First edition 2017-10 Health informatics Personal health device communication - Part 10422: Device specialization Urine analyser Informatique de santé - Communication entre dispositifs de santé personnels- Partie 10422: Specialisation des dispositifs - Analyseur d'urine [so Reference number IS0/IEEE11073-10422:2017(E) 3331@ @IEEE2016 xing permitted without license from IHS Not for Resale, 11/07/2017 09:12:45 MST IS0/IEEE11073-10422:2017(E) COPYRIGHTPROTECTEDDOCUMENT @IEEE2016 Allrightsreserved.Unless otherwise specified,nopartofthispublicationmaybereproducedorutilized otherwiseinanyformor permission. Permission can be requested from either ISO or IEEE at the address below or ISO's member body in the country of the requester. ISO copyright office Institute of Electrical and Electronics Engineers, Inc Ch. de Blandonnet 8 . CP 401 3 Park Avenue, New York CH-1214 Vernier, Geneva, Switzerland NY10016-5997,USA Tel. +41 22 749 01 11 Fax +4122749 0947 [email protected] [email protected] www.iso.org www.ieee.org @ IEEE 2016 - All rights reserved Not for Resale, 11/07/2017 09:12:45 MST IS0/IEEE 11073-10422:2017(E) Foreword (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 ElectrotechnicalCommission(iEC)onallmattersofelectrotechnicalstandardization. IEEE Standards documents are developed within the IEEE Societies and the Standards Coordinating Committeesof theIEEE StandardsAssociation(IEEE-SA)StandardsBoard.TheIEEEdevelopsitsstandards throughaconsensusdevelopmentprocess,approvedbytheAmericanNationalStandardsInstitute,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. 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 International Standard requires approval by at least 75 % of the member bodies casting a vote. covered by patent rights. By publication of this standard, no position is taken with respect to the existence or 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 connectionwithsubmissionofaLetterofAssuranceoraPatentStatementandLicensingDeclarationForm,ifany 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 11073-10422 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 Development Organization cooperation agreement between ISO and IEEE. Both parties are responsible for the maintenance of this document. iii license from Ih Not for Resale, 11/07/2017 09