EN ISO 5832-7:2019

Implants for surgery - Metallic materials - Part 7: Forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy (ISO 5832-7:2016)

ISO 5832-7:2016 specifies the characteristics of, and corresponding test methods for, forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy for use in the manufacture of surgical implants.

Chirurgische Implantate - Metallische Werkstoffe - Teil 7: Schmiedbare und kaltumformbare Cobalt-Chrom-Nickel-Molybdän-Eisenlegierung (ISO 5832-7:2016)

Dieses Dokument legt Eigenschaften und die entsprechenden Prüfverfahren für eine schmiedbare und kaltumformbare Cobalt Chrom Nickel Molybdän Eisenlegierung fest, die zur Herstellung von chirurgischen Implantaten verwendet wird.
ANMERKUNG   Die mechanischen Eigenschaften einer Probe aus einem Fertigprodukt, welches aus dieser Legierung hergestellt wurde, stimmen nicht notwendigerweise mit den in diesem Dokument festgelegten Eigenschaften überein.

Implants chirurgicaux - Produits à base de métaux - Partie 7: Alliage à forger mis en forme à froid à base de cobalt, de chrome, de nickel, de molybdène et de fer (ISO 5832-7:2016)

L'ISO 5832-7 :2016 définit les caractéristiques et les méthodes d'essai correspondantes de l'alliage à forger mis en forme à froid à base de cobalt, de chrome, de nickel, de molybdène et de fer utilisé pour fabriquer des implants chirurgicaux.

Vsadki (implantati) za kirurgijo - Kovinski materiali - 7. del: Kovne in hladno oblikovane kobalt-krom-nikelj-molibden-železove zlitine (ISO 5832-7:2016)

Standard ISO 5832-7:2016 določa lastnosti in zadevne preskusne metode za kovne ter hladno oblikovane kobalt-krom-nikelj-molibden-železove zlitine, ki se uporabljajo pri izdelavi vsadkov (implantatov) za kirurgijo.

General Information

• Status: Withdrawn
• Publication Date: 01-Oct-2019
• Withdrawal Date: 16-Apr-2024
• 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: 02-Oct-2019
• Due Date: 28-Jul-2020
• Completion Date: 02-Oct-2019
• Ref Project: SIST EN ISO 5832-7:2019 - Implants for surgery - Metallic materials - Part 7: Forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy (ISO 5832-7:2016)

Relations

• Replaced By: EN ISO 5832-7:2024 - Implants for surgery - Metallic materials - Part 7: Forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy (ISO 5832-7:2024)
• Effective Date: 06-Oct-2021

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 5832-7:2019
01-december-2019
Vsadki (implantati) za kirurgijo - Kovinski materiali - 7. del: Kovne in hladno
oblikovane kobalt-krom-nikelj-molibden-železove zlitine (ISO 5832-7:2016)
Implants for surgery - Metallic materials - Part 7: Forgeable and cold-formed cobalt-
chromium-nickel-molybdenum-iron alloy (ISO 5832-7:2016)
Chirurgische Implantate - Metallische Werkstoffe - Teil 7: Schmiedbare und
kaltumformbare Cobalt-Chrom-Nickel-Molybdän-Eisenlegierung (ISO 5832-7:2016)
Implants chirurgicaux - Produits à base de métaux - Partie 7: Alliage à forger mis en
forme à froid à base de cobalt, de chrome, de nickel, de molybdène et de fer (ISO 5832-
7:2016)
Ta slovenski standard je istoveten z: EN ISO 5832-7:2019
ICS:
11.040.40 Implantanti za kirurgijo, Implants for surgery,
protetiko in ortetiko prosthetics and orthotics
SIST EN ISO 5832-7:2019 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 5832-7:2019

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SIST EN ISO 5832-7:2019


EN ISO 5832-7
EUROPEAN STANDARD

NORME EUROPÉENNE

October 2019
EUROPÄISCHE NORM
ICS 11.040.40
English Version

Implants for surgery - Metallic materials - Part 7:
Forgeable and cold-formed cobalt-chromium-nickel-
molybdenum-iron alloy (ISO 5832-7:2016)
Implants chirurgicaux - Produits à base de métaux - Chirurgische Implantate - Metallische Werkstoffe - Teil
Partie 7: Alliage à forger mis en forme à froid à base de 7: Schmiedbare und kaltumformbare Cobalt-Chrom-
cobalt, de chrome, de nickel, de molybdène et de fer Nickel-Molybdän-Eisenlegierung (ISO 5832-7:2016)
(ISO 5832-7:2016)
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 5832-7:2019 E
worldwide for CEN national Members.

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SIST EN ISO 5832-7:2019
EN ISO 5832-7:2019 (E)
Contents Page
European foreword . 3

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SIST EN ISO 5832-7:2019
EN ISO 5832-7:2019 (E)
European foreword
The text of ISO 5832-7:2016 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 5832-7:2019 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
...