EN ISO 5832-3-2016 en Implants for surgery - Metallic materials - Part 3 Wrought titanium 6-aluminium 4-vanadium alloy《外科植入物金属材料第3部分 锻造钛-6铝四钒合金(ISO 5832-3 2016)》.pdf
《EN ISO 5832-3-2016 en Implants for surgery - Metallic materials - Part 3 Wrought titanium 6-aluminium 4-vanadium alloy《外科植入物金属材料第3部分 锻造钛-6铝四钒合金(ISO 5832-3 2016)》.pdf》由会员分享,可在线阅读,更多相关《EN ISO 5832-3-2016 en Implants for surgery - Metallic materials - Part 3 Wrought titanium 6-aluminium 4-vanadium alloy《外科植入物金属材料第3部分 锻造钛-6铝四钒合金(ISO 5832-3 2016)》.pdf(18页珍藏版)》请在麦多课文档分享上搜索。
1、BS EN ISO 5832-3:2016Implants for surgery Metallic materialsPart 3: Wrought titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:2016)BSI Standards PublicationWB11885_BSI_StandardCovs_2013_AW.indd 1 15/05/2013 15:06BS EN ISO 5832-3:2016 BRITISH STANDARDNational forewordThis British Standard is the UK i
2、mplementation of EN ISO 5832-3:2016. It supersedes BS EN ISO 5832-3:2012 which iswithdrawn.The UK participation in its preparation was entrusted to Technical Committee CH/150/1, Materials for surgical implants.A list of organizations represented on this committee can be obtained on request to its se
3、cretary.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 2016.Published by BSI Standards Limited 2016ISBN 978 0 580 87493 2 ICS 11.040.40 Compliance with a British Standard ca
4、nnot confer immunity from legal obligations.This British Standard was published under the authority of the Standards Policy and Strategy Committee on 30 November 2016.Amendments/corrigenda issued since publicationDate T e x t a f f e c t e dEUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN ISO 58
5、32-3 November 2016 ICS 11.040.40 Supersedes EN ISO 5832-3:2012English Version Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:2016) Implants chirurgicaux - Produits base de mtaux - Partie 3: Alliage corroy base de titane, daluminium-6 et
6、de vanadium-4 (ISO 5832-3:2016) Chirurgische Implantate - Metallische Werkstoffe - Teil 3: Titan 6-Aluminium 4-Vanadium Knetlegierung (ISO 5832-3:2016) This European Standard was approved by CEN on 12 September 2016. CEN members are bound to comply with the CEN/CENELEC Internal Regulations which sti
7、pulate 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 CEN member. This European
8、 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 versions. CEN members are th
9、e 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, Poland, Portugal, Romani
10、a, 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 2016 CEN All rights of exploitation in any form and by a
11、ny means reserved worldwide for CEN national Members. Ref. No. EN ISO 5832-3:2016 EBS EN ISO 5832-3:2016EN ISO 5832-3:2016 (E) 3 European foreword This document (EN ISO 5832-3:2016) has been prepared by Technical Committee ISO/TC 150 “Implants for surgery” in collaboration with Technical Committee C
12、EN/TC 55 “Dentistry” the secretariat of which is held by DIN. 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 May 2017, and conflicting national standards shall be withdrawn at the latest by May 2
13、017. 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 patent rights. This document supersedes EN ISO 5832-3:2012. According to the CEN-CENELEC Interna
14、l 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, France, Germany, Greece, Hungary, Iceland, Irel
15、and, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. Endorsement notice The text of ISO 5832-3:2016 has been approved by CEN as EN ISO 5832-3:2016 without any modification. BS
16、EN ISO 5832-3:2016ISO 5832-3:2016(E)Foreword ivIntroduction v1 Scope . 12 Normative references 13 Terms and definitions . 14 Chemical composition . 15 Microstructure 26 Mechanical properties 26.1 Tensile . 26.2 Bending 37 Test methods . 3Annex A (normative) Catalogues of metallographic micrographs o
17、f typical alpha+beta titanium microstructures 4Annex B (informative) Mechanical Properties Harmonization between ISO and ASTM wrought titanium 6-aluminium 4-vanadium Implant Material Standards . 5Bibliography 7 ISO 2016 All rights reserved iiiContents PageBS EN ISO 5832-3:2016ISO 5832-3:2016(E)Forew
18、ordISO (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 technic
19、al 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 (IEC) on all matters of el
20、ectrotechnical 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 be noted. This document was
21、 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 identifying any or all such paten
22、t 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 convenience of users and does not co
23、nstitute an endorsement.For an explanation on the meaning of ISO specific terms and expressions related to conformity assessment, as well as information about ISOs adherence to the World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see the following URL: www.iso.org/i
24、so/foreword.html.The committee responsible for this document is ISO/TC 150, Implants for surgery, Subcommittee SC 1, Materials.This fourth edition cancels and replaces the third edition (ISO 5832-3:1996), which has been technically revised.ISO 5832 consists of the following parts, under the general
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