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
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 5832-7:2019
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 5832-7:2016 has been approved by CEN as EN ISO 5832-7:2019 without any

modification.
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SIST EN ISO 5832-7:2019
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SIST EN ISO 5832-7:2019
INTERNATIONAL ISO
STANDARD 5832-7
Third edition
2016-11-15
Implants for surgery — Metallic
materials —
Part 7:
Forgeable and cold-formed cobalt-
chromium-nickel-molybdenum-iron
alloy
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
Reference number
ISO 5832-7:2016(E)
ISO 2016
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SIST EN ISO 5832-7:2019
ISO 5832-7:2016(E)
COPYRIGHT PROTECTED DOCUMENT
© ISO 2016, Published in Switzerland

All rights reserved. Unless otherwise specified, 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
Ch. de Blandonnet 8 • CP 401
CH-1214 Vernier, Geneva, Switzerland
Tel. +41 22 749 01 11
Fax +41 22 749 09 47
copyright@iso.org
www.iso.org
ii © ISO 2016 – All rights reserved
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SIST EN ISO 5832-7:2019
ISO 5832-7:2016(E)
Contents Page

Foreword ........................................................................................................................................................................................................................................iv

Introduction ..................................................................................................................................................................................................................................v

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

2 Normative references ...................................................................................................................................................................................... 1

3 Terms and definitions ..................................................................................................................................................................................... 1

4 Chemical composition ..................................................................................................................................................................................... 1

...

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