EN ISO 5832-3:2016

Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:2016)

ISO 5832-3:2016 specifies the characteristics of, and corresponding test methods for, the wrought titanium alloy known as titanium 6-aluminium 4-vanadium alloy (Ti 6-AI4-V alloy) for use in the manufacture of surgical implants.
NOTE The mechanical properties of a sample obtained from a finished product made of this alloy may not necessarily comply with the specifications given in this part of ISO 5832.

Chirurgische Implantate - Metallische Werkstoffe - Teil 3: Titan 6-Aluminium 4-Vanadium Knetlegierung (ISO 5832-3:2016)

Dieser Teil von ISO 5832 beschreibt die Eigenschaften und dazugehörige Prüfverfahren für die Knetlegierung aus Titan, die als Titan 6-Aluminium 4-Vanadium Legierung (Ti 6-Al 4-V Legierung) bei der Herstellung von chirurgischen Implantaten bekannt ist.
ANMERKUNG   Die mechanischen Eigenschaften einer Probe, die an einem Endprodukt aus diesem Metall erhalten werden, müssen nicht notwendigerweise mit den Angaben in diesem Teil von ISO 5832 übereinstimmen.

Implants chirurgicaux - Produits à base de métaux - Partie 3: Alliage corroyé à base de titane, d'aluminium-6 et de vanadium-4 (ISO 5832-3:2016)

ISO 5832-3:2016 spécifie les caractéristiques de l'alliage corroyé à base de de titane, connu sous le nom d'alliage de titane, d'aluminium-6 et de vanadium-4 (alliage Ti 6-AI4-V) utilisable dans la fabrication d'implants chirurgicaux, et les méthodes d'essai correspondantes.
NOTE Les propriétés mécaniques d'un échantillon prélevé sur un produit fini fabriqué avec cet alliage peuvent ne pas nécessairement être conformes aux spécifications données dans la présente partie de l'ISO 5832.

Vsadki (implantati) za kirurgijo - Kovinski materiali - 3. del: Titanova 6-aluminijeva 4-vanadijeva zlitina (ISO 5832-3:2016)

Določa lastnosti in zadevne preskusne metode za kovano titanovo zlitino, znano kot titanova 6-aluminijeva 4-vanadijeva zlitina (zlitina Ti 6-AI 4-V), iz katere izdelujejo vsadke za kirurgijo.

General Information

• Status: Withdrawn
• Publication Date: 08-Nov-2016
• Withdrawal Date: 30-Nov-2021
• 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: 01-Dec-2021
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Ref Project: SIST EN ISO 5832-3:2017 - Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:2016)

Relations

• Replaces: EN ISO 5832-3:2012 - Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:1996)
• Effective Date: 08-Jun-2022
• Replaced By: EN ISO 5832-3:2021 - Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-vanadium alloy (ISO 5832-3:2021)
• Effective Date: 08-Jun-2022

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 5832-3:2017
01-april-2017
1DGRPHãþD
SIST EN ISO 5832-3:2012
Vsadki (implantati) za kirurgijo - Kovinski materiali - 3. del: Titanova 6-aluminijeva
4-vanadijeva zlitina (ISO 5832-3:2016)
Implants for surgery - Metallic materials - Part 3: Wrought titanium 6-aluminium 4-
vanadium alloy (ISO 5832-3:2016)
Chirurgische Implantate - Metallische Werkstoffe - Teil 3: Titan 6-Aluminium 4-Vanadium
Knetlegierung (ISO 5832-3:2016)
Implants chirurgicaux - Produits à base de métaux - Partie 3 : Alliage à forger à base de
titane, d'aluminium 6 et de vanadium 4 (ISO 5832-3:2016)
Ta slovenski standard je istoveten z: EN ISO 5832-3:2016
ICS:
11.040.40 Implantanti za kirurgijo, Implants for surgery,
protetiko in ortetiko prosthetics and orthotics
SIST EN ISO 5832-3:2017 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 5832-3:2017

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SIST EN ISO 5832-3:2017


EN ISO 5832-3
EUROPEAN STANDARD

NORME EUROPÉENNE

November 2016
EUROPÄISCHE NORM
ICS 11.040.40 Supersedes EN ISO 5832-3:2012
English Version

Implants for surgery - Metallic materials - Part 3: Wrought
titanium 6-aluminium 4-vanadium alloy (ISO 5832-
3:2016)
Implants chirurgicaux - Produits à base de métaux - Chirurgische Implantate - Metallische Werkstoffe - Teil
Partie 3: Alliage corroyé à base de titane, d'aluminium- 3: Titan 6-Aluminium 4-Vanadium Knetlegierung (ISO
6 et de vanadium-4 (ISO 5832-3:2016) 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 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, Former Yugoslav Republic of Macedonia, 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

CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2016 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 5832-3:2016 E
worldwide for CEN national Members.

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SIST EN ISO 5832-3:2017
EN ISO 5832-3:2016 (E)
Contents Page
European foreword . 3

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SIST EN ISO 5832-3:2017
EN ISO 5832-3:2016 (E)
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 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 May 2017, and conflicting national standards shall be
withdrawn at the latest by May 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 patent
rights.
This document supersedes EN ISO 5832-3:2012.
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,
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 5832-3:2016 has been approved by CEN as EN ISO 5832-3:2016 without any
modification.
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