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CEN

EN ISO 5832-6:2019

(Main)

Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy (ISO 5832-6:1997)

Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy (ISO 5832-6:1997)

This part of ISO 5832 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 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 6: Kobalt-Nickel-Chrom-Molybdän-Schmiedelegierung (ISO 5832-6:1997)

Dieser Teil der ISO 5832 legt die Eigenschaften von und die entsprechenden Prüfverfahren für die geschmiedete Kobalt Nickel Chrom Molybdän Legierung fest, die zur Herstellung von chirurgischen Implantaten verwendet wird.
ANMERKUNG   Die mechanischen Eigenschaften einer Probe eines Fertigproduktes aus dieser Legierung, braucht nicht notwendigerweise mit den festgelegten Eigenschaften dieses Teils von ISO 5832 übereinstimmen.

Implants chirurgicaux - Produits à base de métaux - Partie 6: Alliage corroyé à base de cobalt, de nickel, de chrome et de molybdène (ISO 5832-6:1997)

La présente partie de l'ISO 5832 prescrit les caractéristiques et les méthodes d'essai correspondantes pour l'alliage corroyé à base de cobalt, de nickel, de chrome et de molybdène utilisé pour la fabrication des implants chirurgicaux.
NOTE -- Les caractéristiques mécaniques d'un échantillon prélevé sur un produit fini fabriqué avec cet alliage peuvent ne pas être nécessairement conformes aux valeurs données dans la présente partie de l'ISO 5832.

Vsadki (implantati) za kirurgijo - Kovinski materiali - 6. del: Kobalt-nikelj-krom-molibdenova kovana zlitina (ISO 5832-6:1997)

Ta del standarda ISO 5832 določa lastnosti in zadevne preskusne metode za kobalt-nikelj-krom-molibdenovo kovano zlitino, ki se uporablja pri izdelavi vsadkov (implantatov) za kirurgijo.
OPOMBA: Mehanske lastnosti vzorca končnega izdelka iz te zlitine niso nujno
v skladu s specifikacijami v tem delu standarda ISO 5832.

General Information

Status
Withdrawn
Publication Date
01-Oct-2019
Withdrawal Date
29-Mar-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
9960 - Withdrawal effective - Withdrawal
Completion Date
30-Mar-2022
Ref Project
SIST EN ISO 5832-6:2019 - Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy (ISO 5832-6:1997)

Relations

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

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SLOVENSKI STANDARD
SIST EN ISO 5832-6:2019
01-december-2019
Vsadki (implantati) za kirurgijo - Kovinski materiali - 6. del: Kobalt-nikelj-krom-
molibdenova kovana zlitina (ISO 5832-6:1997)
Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-
molybdenum alloy (ISO 5832-6:1997)
Chirurgische Implantate - Metallische Werkstoffe - Teil 6: Kobalt-Nickel-Chrom-Molybdän
Schmiedelegierung (ISO 5832-6:1997)
Implants chirurgicaux - Produits à base de métaux - Partie 6: Alliage corroyé à base de
cobalt, de nickel, de chrome et de molybdène (ISO 5832-6:1997)
Ta slovenski standard je istoveten z: EN ISO 5832-6:2019
ICS:
11.040.40 Implantanti za kirurgijo, Implants for surgery,
protetiko in ortetiko prosthetics and orthotics
SIST EN ISO 5832-6:2019 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 5832-6:2019

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SIST EN ISO 5832-6:2019


EN ISO 5832-6
EUROPEAN STANDARD

NORME EUROPÉENNE

October 2019
EUROPÄISCHE NORM
ICS 11.040.40
English Version

Implants for surgery - Metallic materials - Part 6: Wrought
cobalt-nickel-chromium-molybdenum alloy (ISO 5832-
6:1997)
Implants chirurgicaux - Produits à base de métaux - Chirurgische Implantate - Metallische Werkstoffe - Teil
Partie 6: Alliage corroyé à base de cobalt, de nickel, de 6: Kobalt-Nickel-Chrom-Molybdän-Schmiedelegierung
chrome et de molybdène (ISO 5832-6:1997) (ISO 5832-6:1997)
This European Standard was approved by CEN on 2 September 2019.

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
© 2019 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 5832-6:2019 E
worldwide for CEN national Members.

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SIST EN ISO 5832-6:2019
EN ISO 5832-6:2019 (E)
Contents Page
European foreword . 3

2

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SIST EN ISO 5832-6:2019
EN ISO 5832-6:2019 (E)
European foreword
The text of ISO 5832-6:1997 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 5832-6:2019 by 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 April 2020, and conflicting national standards shall be
withdrawn at the latest by April 2020.
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.
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.
Endorsement notice
The text of ISO 5832-6:1997 has been approved by CEN as EN ISO 5832-6:2019 without any
modification.


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SIST EN ISO 5832-6:2019

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