ISO/IEEE INTERNATIONAL STANDARD 11073-10424 First edition 2016-06-15 Health informatics Personal health device communication - Part 10424: Device Specialization Sleep Apnoea Breathing Therapy Equipment (SABTE) Informatique de santé - Communication entre dispositifs de santé personnels Partie 10424: Spécialisation de dispositif—Equipement de therapie respiratoire de I'apnée du sommeil (SABTE) Referencenumber ISO ISO/IEEE11073-10424:2016(E) 3331 @ ISO 2016 @IEEE2014 ISO/IEEE11073-10424:2016(E) COPYRIGHTPROTECTEDDOCUMENT @IEEE2014 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying and microfilm, without permission in writing from either ISO or IEEE at the respective address below. ISO copyright office Institute of Electrical and Electronics Engineers, Inc. Case postale 56 . CH-1211 Geneva 20 3 Park Avenue, New York NY 10016-5997, USA Tel. + 41 22 749 01 11 E-mail [email protected] Fax + 41 22 749 09 47 Web www.ieee.org E-mail [email protected] Web www.iso.org Published in Switzerland @ ISO 2016 - All rights reserved @ IEEE 2014 - All rights reserved d by IHS unde nited without license from IHS ISO/IEEE 11073-10424:2016(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 non-governmental,inliaisonwithIsO,alsotakepartinthework.IsOcollaboratescloselywiththeInternational ElectrotechnicalCommission(lEC)onallmattersofelectrotechnicalstandardization. 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. 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. Attention is called to the possibility that implementation of this standard may require the use of subject matter 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/lEEE is not responsible for identifying essential 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 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. ISO/IEEE 11073-10424 was prepared by the IEEE 11073 Standards Comittee of the IEEE Engineering in Medicine and Biology Society (as IEEE Std 11073-10424-2014). It was adopted by Technical Committee ISO/TC 215, 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