SIST 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 cobaltnickel 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 die geschmiedete Kobalt-Nickel-Chrom-Molybdän-Legierung fest, die zur Herstellung von chirurgischen Implantaten verwendet wird.
ANMERKUNG Die mechanischen Eigenschaften einer Probe, die einem Fertigprodukt aus der hier beschriebenen Legierung entnommen wurde, können von denen in diesem Dokument festgelegten abweichen.
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
Relations
Standards Content (Sample)
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.
Endorsement notice
The text of ISO 5832-6:2022 has been approved by CEN as EN ISO 5832-6:2022 without any
modification.
3
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SIST EN ISO 5832-6:2022
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SIST EN ISO 5832-6:2022
INTERNATIONAL ISO
STANDARD 5832-6
Third edition
2022-03
Implants for surgery — Metallic
materials —
Part 6:
Wrought cobalt-nickel-chromium-
molybdenum alloy
Implants chirurgicaux — Matériaux métalliques —
Partie 6: Alliage corroyé à base de cobalt, de nickel, de chrome et de
molybdène
Reference number
ISO 5832-6:2022(E)
© ISO 2022
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SIST EN ISO 5832-6:2022
ISO 5832-6:2022(E)
COPYRIGHT PROTECTED DOCUMENT
© ISO 2022
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting on
the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address below
or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii
© ISO 2022 – All rights reserved
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SIST EN ISO 5832-6:2022
ISO 5832-6:2022(E)
Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Chemical composition .1
5 Microstructure. 2
5.1 General . 2
5.2 Grain size index . 2
6 Tensile properties .
...
SLOVENSKI STANDARD
oSIST prEN ISO 5832-6:2021
01-april-2021
Vsadki (implantati) za kirurgijo - Kovinski materiali - 6. del: Kobalt-nikelj-krom-
molibdenova kovana zlitina (ISO/DIS 5832-6:2021)
Implants for surgery - Metallic materials - Part 6: Wrought cobalt-nickel-chromium-
molybdenum alloy (ISO/DIS 5832-6:2021)
Chirurgische Implantate - Metallische Werkstoffe - Teil 6: Kobalt-Nickel-Chrom-
Molybdän-Schmiedelegierung (ISO/DIS 5832-6:2021)
Implants chirurgicaux - Produits à base de métaux - Partie 6: Alliage corroyé à base de
cobalt, de nickel, de chrome et de molybdène (ISO/DIS 5832-6:2021)
Ta slovenski standard je istoveten z: prEN ISO 5832-6
ICS:
11.040.40 Implantanti za kirurgijo, Implants for surgery,
protetiko in ortetiko prosthetics and orthotics
oSIST prEN ISO 5832-6:2021 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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oSIST prEN ISO 5832-6:2021
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oSIST prEN ISO 5832-6:2021
DRAFT INTERNATIONAL STANDARD
ISO/DIS 5832-6
ISO/TC 150/SC 1 Secretariat: DIN
Voting begins on: Voting terminates on:
2021-02-11 2021-05-06
Implants for surgery — Metallic materials —
Part 6:
Wrought cobalt-nickel-chromium-molybdenum alloy
Implants chirurgicaux — Produits à base de métaux —
Partie 6: Alliage corroyé à base de cobalt, de nickel, de chrome et de molybdène
ICS: 11.040.40
THIS DOCUMENT IS A DRAFT CIRCULATED
This document is circulated as received from the committee secretariat.
FOR COMMENT AND APPROVAL. IT IS
THEREFORE SUBJECT TO CHANGE AND MAY
NOT BE REFERRED TO AS AN INTERNATIONAL
STANDARD UNTIL PUBLISHED AS SUCH.
IN ADDITION TO THEIR EVALUATION AS
ISO/CEN PARALLEL PROCESSING
BEING ACCEPTABLE FOR INDUSTRIAL,
TECHNOLOGICAL, COMMERCIAL AND
USER PURPOSES, DRAFT INTERNATIONAL
STANDARDS MAY ON OCCASION HAVE TO
BE CONSIDERED IN THE LIGHT OF THEIR
POTENTIAL TO BECOME STANDARDS TO
WHICH REFERENCE MAY BE MADE IN
Reference number
NATIONAL REGULATIONS.
ISO/DIS 5832-6:2021(E)
RECIPIENTS OF THIS DRAFT ARE INVITED
TO SUBMIT, WITH THEIR COMMENTS,
NOTIFICATION OF ANY RELEVANT PATENT
RIGHTS OF WHICH THEY ARE AWARE AND TO
©
PROVIDE SUPPORTING DOCUMENTATION. ISO 2021
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oSIST prEN ISO 5832-6:2021
ISO/DIS 5832-6:2021(E)
COPYRIGHT PROTECTED DOCUMENT
© ISO 2021
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2021 – All rights reserved
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oSIST prEN ISO 5832-6:2021
ISO/DIS 5832-6:2021(E)
Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Chemical composition . 1
5 Microstructure . 2
5.1 General . 2
5.2 Grain size index . 2
6 Mechanical properties . 2
7 Test methods . 3
© ISO 2021 – All rights reserved iii
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oSIST prEN ISO 5832-6:2021
ISO/DIS 5832-6:2021(E)
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/ directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject
...
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