EN ISO 5832-3:2012

Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:1996)

Specifies the characteristics of, and corresponding test methods for, the wrought titanium alloy known as titanium 6-aluminium 4-vanadium alloy (Ti 6-Al 4-V alloy) for use in the manufacture of surgical implants.

Chirurgische Implantate - Metallische Werkstoffe - Teil 3: Titan 6-Aluminium 4-Vanadium Knetlegierungen (ISO 5832-3:1996)

Dieser Teil von ISO 5832 beschreibt Eigenschaften und legt dazugehörige Prüfverfahren für Titan-Knetlegierung fest, die als Titan 6-Aluminium 4-Vanadium Legierung (Ti 6-Al 4-V Legierung) bekannt ist und zur Herstellung von chirurgischen Implantaten verwendet wird.
ANMERKUNG 1   Die mechanischen Eigenschaften einer Probe, die von einem Fertigprodukt aus diesem Metall entnommen wurden, müssen nicht notwendigerweise mit denen in diesem Teil von ISO 5832 angegebenen übereinstimmen.

Implants chirurgicaux - Produits à base de métaux - Partie 3: Alliage à forger à base de titane, d'aluminium 6 et de vanadium 4 (ISO 5832-3:1996)

Vsadki (implantati) za kirurgijo - Kovinski materiali - 3. del: Kovana zlitina (ISO 5832-3:1996)

Ta del standarda ISO 5832 določa lastnosti in zadevne preskusne metode za kovano titanovo zlitino, znano kot zlitina Ti 6-AI 4-V, iz katere izdelujejo vsadke za kirurgijo.

General Information

• Status: Withdrawn
• Publication Date: 22-May-2012
• Withdrawal Date: 08-Nov-2016
• ICS: 11.040.40 - Implants for surgery, prosthetics and orthotics
• ICS: 77.120.50 - Titanium and titanium alloys
• Technical Committee: CEN/TC 55 - Dentistry
• Drafting Committee: CEN/TC 55 - Dentistry
• Current Stage: 9960 - Withdrawal effective - Withdrawal
• Completion Date: 09-Nov-2016
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Ref Project: SIST EN ISO 5832-3:2012 - Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:1996)

Relations

• Replaced By: EN ISO 5832-3:2016 - Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:2016)
• Effective Date: 08-Jun-2022

Standards Content (Sample)

SLOVENSKI STANDARD
01-oktober-2012
Vsadki (implantati) za kirurgijo - Kovinski materiali - 3. del: Kovana zlitina (ISO
5832-3:1996)
Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-
vanadium alloy (ISO 5832-3:1996)
Chirurgische Implantate - Metallische Werkstoffe - Teil 3: Titan 6-Aluminium 4-Vanadium
Knetlegierungen (ISO 5832-3:1996)
Implants chirurgicaux - Produits à base de métaux - Partie 3: Alliage à forger à base de
titane, d'aluminium 6 et de vanadium 4 (ISO 5832-3:1996)
Ta slovenski standard je istoveten z: EN ISO 5832-3:2012
ICS:
11.040.40 Implantanti za kirurgijo, Implants for surgery,
protetiko in ortetiko prosthetics and orthotics
77.120.50 Titan in titanove zlitine Titanium and titanium alloys
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EUROPEAN STANDARD
EN ISO 5832-3
NORME EUROPÉENNE
EUROPÄISCHE NORM
May 2012
ICS 11.040.40
English Version
Implants for surgery - Metallic materials - Part 3: Wrought
titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:1996)
Implants chirurgicaux - Produits à base de métaux - Partie Chirurgische Implantate - Metallische Werkstoffe - Teil 3:
3: Alliage à forger à base de titane, d'aluminium 6 et de Titan 6-Aluminium 4-Vanadium Knetlegierungen (ISO
vanadium 4 (ISO 5832-3:1996) 5832-3:1996)
This European Standard was approved by CEN on 28 April 2012.

CEN members are bound to comply with the CEN/CENELEC Internal 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 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 versions.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland,
Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom.

EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2012 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 5832-3:2012: E
worldwide for CEN national Members.

Contents Page
Foreword .3

Foreword
The text of ISO 5832-3:1996 has been prepared by Technical Committee ISO/TC 150 “Implants for surgery” of
the International Organization for Standardization (ISO) and has been taken over as EN ISO 5832-3:2012 by
Technical Committee CEN/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 November 2012, and conflicting national standards shall be withdrawn
at the latest by November 2012.
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.
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, France, Germany, Greece, Hungary, Iceland, Ireland, 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 5832-3:1996 has been approved by CEN as a EN ISO 5832-3:2012 without any modification.

INTERNATIONAL
ISO
STANDARD 5832-3
Third edition
1996-07-01
lmplants for surgery - Metallic materials -
Part 3:
Wrought titanium 6-aluminium 4-vanadium alloy
Implants chirurgicaux - Produits à base de métaux -
Partie 3: Alliage à forger à base de titane, d’aluminium 6 et de vanadium 4
Reference number
ISO 5832-3 : 1996(E)
ISO 5832-3: 1996(E)
Foreword
ISO (the International Organization for Standardization) is a worldwide
federation of national standards bodies (60 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 rep-
resented 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 electrotechnical standardization.
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.
International Standard ISO 5832-3 was prepared by Technical Committee
ISO/TC 150, Implants for surgery, Subcommittee SC 1, M&eria/s.
This third edition cancels and replaces the second edition
(ISO 5832-3:1990), which has been technically revised.
ISO 5832 consists of the following parts, under the general title Implants
for surgery - Me tallic ma terials:
- Part 7: Wrought stainless steel
- P
...