EN ISO 5832-2:2012

Implants for surgery - Metallic materials - Part 2: Unalloyed titanium (ISO 5832-2:1999)

This document specifies the characteristics of, and corresponding test methods for, unalloyed titanium for use in the manufacture of surgical and dental implants.

Chirurgische Implantate - Metallische Werkstoffe - Teil 2: Unlegiertes Titan (ISO 5832-2:1999)

Dieser Teil von ISO 5832 beschreibt Eigenschaften und dazugehörige Prüfverfahren für unlegiertes Titan, das zur Herstellung von chirurgischen Implantaten verwendet wird.
Es werden Festlegungen für sechs verschiedene Titan-Güten auf der Basis der Zugfestigkeit getroffen (siehe Tabelle 2).
ANMERKUNG- 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 2: Titane non allié (ISO 5832-2:1999, Version corrigée 2012-07-01)

L'ISO 5832-2:1999 spécifie les caractéristiques du titane non allié utilisé pour la fabrication des implants chirurgicaux et les méthodes d'essai correspondantes.

Vsadki (implantati) za kirurgijo - Kovinski materiali - 2. del: Nelegirani titan (ISO 5832-2:1999)

Ta del standarda ISO 5832 določa lastnosti in zadevne preskusne metode za nelegirani titan, ki se uporablja pri izdelavi vsadkov za kirurgijo. Predpisi so pripravljeni za šest stopenj natezne trdnosti titana (preglednica 2). OPOMBA: mehanske lastnosti vzorca končnega izdelka iz te kovine niso nujno v skladu z lastnostmi, ki so določene v tem delu standarda ISO 5832.

General Information

• Status: Withdrawn
• Publication Date: 22-May-2012
• Withdrawal Date: 01-May-2018
• 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: 02-May-2018
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Ref Project: SIST EN ISO 5832-2:2012 - Implants for surgery - Metallic materials - Part 2: Unalloyed titanium (ISO 5832-2:1999)

Relations

• Replaced By: EN ISO 5832-2:2018 - Implants for surgery - Metallic materials - Part 2: Unalloyed titanium (ISO 5832-2:2018)
• Effective Date: 04-May-2016

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 5832-2:2012
01-oktober-2012
Vsadki (implantati) za kirurgijo - Kovinski materiali - 2. del: Nelegirani titan (ISO
5832-2:1999)
Implants for surgery - Metallic materials - Part 2: Unalloyed titanium (ISO 5832-2:1999)
Chirurgische Implantate - Metallische Werkstoffe - Teil 2: Unlegiertes Titan (ISO 5832-
2:1999)
Implants chirurgicaux - Produits à base de métaux - Partie 2: Titane non allié (ISO 5832-
2:1999)
Ta slovenski standard je istoveten z: EN ISO 5832-2:2012
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
SIST EN ISO 5832-2:2012 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 5832-2:2012

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SIST EN ISO 5832-2:2012


EUROPEAN STANDARD
EN ISO 5832-2

NORME EUROPÉENNE

EUROPÄISCHE NORM
May 2012
ICS 11.040.40
English Version
Implants for surgery - Metallic materials - Part 2: Unalloyed
titanium (ISO 5832-2:1999)
Implants chirurgicaux - Produits à base de métaux - Partie Chirurgische Implantate - Metallische Werkstoffe - Teil 2:
2: Titane non allié (ISO 5832-2:1999) Unlegiertes Titan (ISO 5832-2:1999)
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 5832-2:2012: E
worldwide for CEN national Members.

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SIST EN ISO 5832-2:2012
EN ISO 5832-2:2012 (E)
Contents Page
Foreword .3

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SIST EN ISO 5832-2:2012
EN ISO 5832-2:2012 (E)
Foreword
The text of ISO 5832-2:1999 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 5832-2:2012 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 5832-2:1999 has been approved by CEN as a EN ISO 5832-2:2012 without any modification.

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SIST EN ISO 5832-2:2012

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SIST EN ISO 5832-2:2012
INTERNATIONAL ISO
STANDARD 5832-2
First edition
1999-07-15
Implants for surgery — Metallic materials —
Part 2:
Unalloyed titanium
Implants chirurgicaux — Produits à base de métaux —
Partie 2: Titane non allié
A
Reference num
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