BS PD ISO TS 16955-2016 Prosthetics Quantification of physical parameters of ankle foot devices and foot units《假肢 踝足器械和足装置的物理参数量化》.pdf
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1、Prosthetics Quantification of physical parameters of ankle foot devices and foot units PD ISO/TS 16955:2016 BSI Standards Publication WB11885_BSI_StandardCovs_2013_AW.indd 1 15/05/2013 15:06National foreword T h i s P u b l i s h e d D o c u m e n t i s t h e U K i m p l e m e n t a t i o n o f I S
2、O / T S 1 6 9 5 5 : 2 0 1 6 . The UK participation in its preparation was entrusted to Technical Committee CH/168, Prosthetics and orthotics. 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 necess
3、ary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2016. Published by BSI Standards Limited 2016 ISBN 978 0 580 92002 8 ICS 11.040.40 Compliance with a British Standard cannot confer immunity from legal obligations. This Published Docum
4、ent was published under the authority of the Standards Policy and Strategy Committee on 30 June 2016. Amendments/corrigenda issued since publication Date Text affected PUBLISHED DOCUMENT PD ISO/TS 16955:2016 ISO 2016 Prosthetics Quantification of physical parameters of ankle foot devices and foot un
5、its Prothses Quantification des paramtres physiques des dispositifs de cheville/pied et units pour les pieds TECHNICAL SPECIFICATION ISO/TS 16955 Reference number ISO/TS 16955:2016(E) First edition 2016-06-15 PD ISO/TS 16955:2016 ISO/TS 16955:2016(E)ii ISO 2016 All rights reserved COPYRIGHT PROTECTE
6、D DOCUMENT ISO 2016, Published in Switzerland 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 w
7、ritten permission. Permission can be requested from either ISO at the address below or ISOs member body in the country of the requester. ISO copyright office Ch. de Blandonnet 8 CP 401 CH-1214 Vernier, Geneva, Switzerland Tel. +41 22 749 01 11 Fax +41 22 749 09 47 copyrightiso.org www.iso.org PD ISO
8、/TS 16955:2016 ISO/TS 16955:2016(E)Foreword iv Introduction v 1 Scope . 1 2 Normative references 1 3 Terms and definitions . 1 4 Symbols and abbreviated terms . 2 5 Requirements 2 6 Setup conditions . 2 7 Quantification 3 7.1 Heel, mid-foot and toe characteristics 3 7.1.1 Procedure . 3 7.1.2 Data co
9、llection and calculations . 4 7.2 Roll-over characteristics . 5 7.2.1 Procedure . 5 7.2.2 Data collection and calculations . 6 7.3 Torsional characteristic . 7 7.3.1 Procedure . 7 7.3.2 Data collection and calculations . 8 7.4 Frontal plane characteristics 8 7.4.1 Procedure . 8 7.4.2 Data collection
10、 and calculations . 9 8 Accessories 10 8.1 General 10 8.2 Procedure .10 8.3 Results .10 Annex A (informative) Quick reference 11 Annex B (informative) Three dimensional locus of force contact point on foot-sole .12 Bibliography .17 ISO 2016 All rights reserved iii Contents Page PD ISO/TS 16955:2016
11、ISO/TS 16955:2016(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
12、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
13、 (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
14、 be noted. This document was drafted in accordance with the editorial rules of the ISO/IEC Directives, Part 2 (see www.iso.org/directives). 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 iden
15、tifying 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 conven
16、ience of users and does not constitute an endorsement. For an explanation on the meaning of ISO specific terms and expressions related to conformit y assessment, as well as information about ISOs adherence to the World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see
17、the following URL: www.iso.org/iso/foreword.html. The committee responsible for this document is ISO/TC 168 Prosthetics and orthotics.iv ISO 2016 All rights reserved PD ISO/TS 16955:2016 ISO/TS 16955:2016(E) Introduction Three major factors contribute to foot design: a) shape and size; b) strength r
18、equirements; c) functional performance. Where a) is obvious and defined by the footwear, b) is specified in ISO 22523 referring to ISO 22675 (but is not suitable for use as a guide for the selection of a specific ankle-foot device or foot unit in the prescription of an individual lower limb prosthes
19、is), and c) is addressed in this Technical Specification. The AOPA group of ISO/TC 168 members between 2006 and 2009 carried out work on a method to replace design criteria for prosthetic ankle-foot devices with compliance criteria which would be applicable to both jointed devices and unjointed devi
20、ces with elastic elements. In 2010, the working group “Testing” convened in Seattle, Washington and decided to work on a standard, based on the work of the AOPA group and other international groups. The vision statement was: “To develop a standard which describes quantitative methods to evaluate or
21、assess key performance indicators of prosthetic ankle-foot devices which are correlated to measurable prosthesis user benefit.” The subsequent work on this task has made it clear that it consists of (at least) two elements: firstly, to develop a standard which describes quantitative methods to evalu
22、ate or assess key performance indicators and secondly, to investigate and attempt to establish the correlation between these measures and relevant measures of prosthetic user benefit. This Technical Specification describes solely the quantitative methods to evaluate or assess key performance indicat
23、ors. The following definitions apply in understanding how to implement an ISO International Standard and other normative ISO deliverables (TS, PAS, IWA). “shall” indicates a requirement “should” indicates a recommendation “may” is used to indicate that something is permitted “can” is used to indicat
24、e that something is possible, for example, that an organization or individual is able to do something In 3.3.1 of the ISO/IEC Directives, Part 2 (sixth edition, 2011) defines a requirement as an “expression in the content of a document conveying criteria to be fulfilled if compliance with the docume
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