1、BS ISO/IEEE 11073-10442:2015Health informatics Personalhealth device communicationPart 10442: Device specialization Strength fitness equipment (ISO/IEEE 11073-10442:2015)BS EN ISO 11073-10442:2017BSI Standards PublicationWB11885_BSI_StandardCovs_2013_AW.indd 1 15/05/2013 15:06BS EN ISO 11073-10442:2
2、017 BRITISH STANDARDNational forewordThis British Standard is the UK implementation of EN ISO 11073-10442:2017. It is identical to ISO/IEEE 11073-10442:2015. It supersedes BS ISO/IEEE 11073-10442:2015 which is withdrawn.The UK participation in its preparation was entrusted to Technical Committee IST
3、/35, Health informatics.A list of organizations represented on this committee can be obtained on request to its secretary.This publication does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2017
4、. Published by BSI Standards Limited 2017ISBN 978 0 580 93167 3ICS 35.240.80Compliance with a British Standard cannot confer immunity from legal obligations.This British Standard was published under the authority of the Standards Policy and Strategy Committee on 31 March 2015.Amendments/corrigenda i
5、ssued since publicationDate Text affected31 March 2017 This corrigendum renumbers BS ISO/IEEE 11073-10442:2015 as BS EN ISO 11073-10442:2017EUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN ISO 11073-10442 February 2017 ICS 35.240.80 English Version Health informatics - Personal health device com
6、munication - Part 10442: Device specialization - Strength fitness equipment (ISO/IEEE 11073-10442:2015)Informatique de sant - Communication entre dispositifs mdicaux sur le site des soins - Partie 10442: Spcialisation des dispositifs - quipement de mise en forme musculaire (ISO/IEEE 11073-10442:2015
7、) Medizinische Informatik - Kommunikation von Gerten fr die persnliche Gesundheit - Teil 10442: Gertespezifikation - Fitnessgerte fr das Krafttraining (ISO/IEEE 11073-10442:2015) This European Standard was approved by CEN on 16 January 2017. CEN members are bound to comply with the CEN/CENELEC Inter
8、nal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any
9、CEN member. This European Standard exists in three official versions (English, French, German). A version in any other language made by translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the official ver
10、sions. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway,
11、 Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2017 CEN All rights of
12、exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN ISO 11073-10442:2017 EBS ISO/IEEE 11073-10442:2015ISO/IEEE 11073-10442:201(E) IEEE 20 All rights reserved iiiForeword ISO (the International Organization for Standardization) is a worldwide federation
13、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. I
14、nternational 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. IEEE Standards documents are developed within the IEEE
15、 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 viewp
16、oints 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, t
17、est, 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 Internati
18、onal 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
19、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 lic
20、ensing 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 validit
21、y 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 10442 was prepared by the 11073 Committee of the Engineering in Medicine and Biology Society of the IEEE
22、 (as IEEE 11073-10442-2008). 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 ISO and IEEE. IEEE is re
23、sponsible for the maintenance of this document with participation and input from ISO member bodies. ISO/IEEE 11073 consists of the following parts, under the general title Health informatics Personal health device communication (text in parentheses gives a variant of subtitle): Part 00103: Overview
24、Part 10101: (Point-of-care medical device communication) Nomenclature Part 10102: (Point-of-care medical device communication) Nomenclature Annotated ECG Part 10103: (Point-of-care medical device communication) Nomenclature Implantable device, cardiac Part 10201: (Point-of-care medical device commun
25、ication) Domain information model Part 10404: Device specialization Pulse oximeter EN ISO 11073-10442:2017 (E) 3 European foreword The text of ISO/IEEE 11073-10442:2015 has been prepared by Technical Committee ISO/TC 215 “Health informatics” of the International Organization for Standardization (ISO
26、) and has been taken over as EN ISO 11073-10442:2017 by Technical Committee CEN/TC 251 “Health informatics” the secretariat of which is held by NEN. This European Standard shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by
27、 August 2017, and conflicting national standards shall be withdrawn at the latest by August 2017. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible for identifying any or all such pat
28、ent rights. According to the CEN-CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia,
29、 France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. Endorsement notice The text of ISO/IEEE 11073-10442:2015 has been a
30、pproved by CEN as EN ISO 11073-10442:2017 without any modification. BS EN ISO 11073-10442:2017EN ISO 11073-10442:2017 (E)BS ISO/IEEE 11073-10442:2015ISO/IEEE 11073-10442:201(E) IEEE 20 All rights reserved iiiForeword ISO (the International Organization for Standardization) is a worldwide federation
31、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. I
32、nternational 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. IEEE Standards documents are developed within the IEEE
33、 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 viewp
34、oints 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, t
35、est, 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 Internati
36、onal 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
37、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 lic
38、ensing 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 validit
39、y 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 10442 was prepared by the 11073 Committee of the Engineering in Medicine and Biology Society of the IEEE
40、 (as IEEE 11073-10442-2008). 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 ISO and IEEE. IEEE is re
41、sponsible for the maintenance of this document with participation and input from ISO member bodies. ISO/IEEE 11073 consists of the following parts, under the general title Health informatics Personal health device communication (text in parentheses gives a variant of subtitle): Part 00103: Overview
42、Part 10101: (Point-of-care medical device communication) Nomenclature Part 10102: (Point-of-care medical device communication) Nomenclature Annotated ECG Part 10103: (Point-of-care medical device communication) Nomenclature Implantable device, cardiac Part 10201: (Point-of-care medical device commun
43、ication) Domain information model Part 10404: Device specialization Pulse oximeter BS EN ISO 11073-10442:2017ISO/IEEE 11073-10442:2015(E)BS ISO/IEEE 11073-10442:2015ISO/IEEE 11073-10442:201(E) iv IEEE 20 All rights reserved Part 10406: Device specialization Basic electrocardiograph (ECG) (1- to 3-le
44、ad ECG) Part 10407: Device specialization Blood pressure monitor Part 10408: Device specialization Thermometer Part 10415: Device specialization Weighing scale Part 10417: Device specialization Glucose meter Part 10418: Device specialization International Normalized Ratio (INR) monitor Part 10420: D
45、evice specialization Body composition analyzer Part 10421: Device specialization Peak expiratory flow monitor (peak flow) Part 10441: Device specialization Cardiovascular fitness and activity monitor Part 10442: (Point-of-care medical device communication) Device specialization Strength fitness equi
46、pment Part 10471: Device specialization Independent living activity hub Part 10472: Device specialization Medication monitor Part 20101: (Point-of-care medical device communication) Application profiles Base standard Part 20601: Application profile Optimized exchange protocol Part 30200: (Point-of-c
47、are medical device communication) Transport profile Cable connected Part 30300: (Point-of-care medical device communication) Transport profile Infrared wireless Part 30400: (Point-of-care medical device communication) Interface profile Cabled Ethernet Part 90101: (Point-of-care medical device commun
48、ication) Analytical instruments Point-of-care test Part 91064: (Standard communication protocol) Computer-assisted electrocardiography Part 92001: (Medical waveform format) Encoding rules BS ISO/IEEE 11073-10442:2015IEEE Std 11073-10442-2008Health informaticsPersonal health device communication Part
49、 10442: Device specializationStrength fitness equipment IEEE3 Park Avenue New York, NY 10016-5997, USA9 January 2009IEEE Engineering in Medicine and Biology Society Sponsored by the11073Standard Committee11073-10442TMAuthorized licensed use limited to: IEEE Standards Staff and authorized IEEE Sponsor Ballot Participants. Downloaded on September 25,2013 at 18:30:36 UTC from IEEE Xplore.
