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CEN

EN ISO 5832-6:2022

(Main)

Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy (ISO 5832-6:2022)

Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy (ISO 5832-6:2022)

This document specifies the characteristics of, and corresponding test methods for, wrought cobalt-nickel chromium-molybdenum alloy for use in the manufacture of surgical implants.
NOTE      The tensile properties of a sample obtained from a finished product made of this alloy do not necessarily comply with those specified in this document.

Chirurgische Implantate - Metallische Werkstoffe - Teil 6: Kobalt-Nickel-Chrom-Molybdän-Schmiedelegierung (ISO 5832-6:2022)

Dieses Dokument legt die Eigenschaften von und die entsprechenden Prüfverfahren für geschmiedete Kobalt-Nickel-Chrom-Molybdän-Legierungen fest, die zur Herstellung von chirurgischen Implantaten verwendet werden.
ANMERKUNG   Die Zugeigenschaften einer Probe, die einem Fertigprodukt aus der hier beschriebenen Legierung entnommen wurde, stimmen nicht notwendigerweise mit denen in diesem Dokument festgelegten überein.

Implants chirurgicaux - Matériaux métalliques - Partie 6: Alliage corroyé à base de cobalt, de nickel, de chrome et de molybdène (ISO 5832-6:2022)

Le présent document définit les caractéristiques et les méthodes d'essai correspondantes de l'alliage corroyé à base de cobalt, de nickel, de chrome et de molybdène, utilisé pour fabriquer des implants chirurgicaux.
NOTE      Les caractéristiques d'un échantillon prélevé sur un produit fini fabriqué avec cet alliage ne sont pas nécessairement conformes à celles spécifiées dans le présent document.

Vsadki (implantati) za kirurgijo - Kovinski materiali - 6. del: Kobalt-nikelj-krom-molibdenova kovana zlitina (ISO 5832-6:2022)

Ta dokument določa lastnosti in zadevne preskusne metode za kobalt-nikelj-krom-molibdenovo kovano zlitino, ki se uporablja pri izdelavi vsadkov (implantatov) za kirurgijo.
OPOMBA: Natezne lastnosti vzorca končnega izdelka iz te zlitine niso nujno v skladu z lastnostmi, ki so določene v tem dokumentu.

General Information

Status
Published
Publication Date
29-Mar-2022
Withdrawal Date
29-Sep-2022
ICS
11.040.40 - Implants for surgery, prosthetics and orthotics
Technical Committee
CEN/TC 285 - Non-active surgical implants
Drafting Committee
CEN/TC 285 - Non-active surgical implants
Current Stage
6060 - Definitive text made available (DAV) - Publishing
Start Date
30-Mar-2022
Completion Date
30-Mar-2022
Ref Project
SIST EN ISO 5832-6:2022 - Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy (ISO 5832-6:2022)

Relations

Replaces
EN ISO 5832-6:2019 - Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy (ISO 5832-6:1997)
Effective Date
08-Jun-2022

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SLOVENSKI STANDARD
SIST EN ISO 5832-6:2022
01-junij-2022
Nadomešča:
SIST EN ISO 5832-6:2019
Vsadki (implantati) za kirurgijo - Kovinski materiali - 6. del: Kobalt-nikelj-krom-
molibdenova kovana zlitina (ISO 5832-6:2022)
Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-
molybdenum alloy (ISO 5832-6:2022)
Chirurgische Implantate - Metallische Werkstoffe - Teil 6: Kobalt-Nickel-Chrom-
Molybdän-Schmiedelegierung (ISO 5832-6:2022)
Implants chirurgicaux - Matériaux métalliques - Partie 6: Alliage corroyé à base de
cobalt, de nickel, de chrome et de molybdène (ISO 5832-6:2022)
Ta slovenski standard je istoveten z: EN ISO 5832-6:2022
ICS:
11.040.40 Implantanti za kirurgijo, Implants for surgery,
protetiko in ortetiko prosthetics and orthotics
SIST EN ISO 5832-6:2022 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 5832-6:2022

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SIST EN ISO 5832-6:2022


EN ISO 5832-6
EUROPEAN STANDARD

NORME EUROPÉENNE

March 2022
EUROPÄISCHE NORM
ICS 11.040.40 Supersedes EN ISO 5832-6:2019
English Version

Implants for surgery - Metallic materials - Part 6: Wrought
cobalt-nickel-chromium-molybdenum alloy (ISO 5832-
6:2022)
Implants chirurgicaux - Matériaux métalliques - Partie Chirurgische Implantate - Metallische Werkstoffe - Teil
6: Alliage corroyé à base de cobalt, de nickel, de 6: Kobalt-Nickel-Chrom-Molybdän-Schmiedelegierung
chrome et de molybdène (ISO 5832-6:2022) (ISO 5832-6:2022)
This European Standard was approved by CEN on 20 March 2022.

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, Republic of North Macedonia, Romania, Serbia, 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: Rue de la Science 23, B-1040 Brussels
© 2022 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 5832-6:2022 E
worldwide for CEN national Members.

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SIST EN ISO 5832-6:2022
EN ISO 5832-6:2022 (E)
Contents Page
European foreword . 3

2

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SIST EN ISO 5832-6:2022
EN ISO 5832-6:2022 (E)
European foreword
This document (EN ISO 5832-6:2022) has been prepared by Technical Committee ISO/TC 150
"Implants for surgery" in collaboration with Technical Committee CEN/TC 285 “Non-active surgical
implants” 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 September 2022, and conflicting national standards
shall be withdrawn at the latest by September 2022.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN ISO 5832-6:2019.
Any feedback and questions on this document should be directed to the users’ national standards
body/national committee. A complete listing of these bodies can be found on the CEN website.
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, Republic of
North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the
United Kingdom.
Endo
...

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