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
Published
Public Enquiry End Date
04-Nov-2018
Publication Date
28-Oct-2019
Technical Committee
Current Stage
6060 - National Implementation/Publication (Adopted Project)
Start Date
16-Oct-2019
Due Date
21-Dec-2019
Completion Date
29-Oct-2019

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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

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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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SIST EN ISO 5832-6:2019
INTERNATIONAL
ISO
STANDARD
5832-6
Second edition
1997-07- 15
lmplants for surgery - Metallic materials -
Part 6:
Wrought cobalt-nickel-chromium-molybdenum
alloy
lmplants chirurgicaux - Produits 2 base de mefaux -
Parfie 6: Alliage corroyb 2 base de Cobalt, de nicke/, de chrome et
de molybd&ne
Reference number
ISO 5832-6: 1997(E)
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SIST EN ISO 5832-6:2019
ISO 5832-6: 1997(E)
Page
Contents

1 Scope . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1

2 Normative references . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Chemical composition . . . . . . . . . . . . . . . . . ..*........................................... 1

4 Microstructure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2

.,...................................*................*....... 2
5 Mechanical properties

Test methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2

0 ISO 1997
Unless ot
...

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