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CEN

EN ISO 21536:2007

(Main)

Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO 21536:2007)

Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO 21536:2007)

40.20 desynchronized with ISO due to ISO/CS failure to notify CMC.

Nichtaktive chirurgische Implantate - Implantate zum Gelenkersatz - Besondere Anforderungen an Implantate für den Kniegelenkersatz (ISO 21536:2007)

Diese Internationale Norm legt besondere Anforderungen an Implantate für den Kniegelenksersatz fest. Unter Berücksichtigung der Sicherheit legt diese Internationale Norm Anforderungen an vorgesehene Funktion, Konstruktions¬merkmale, Werkstoffe, Designprüfung, Herstellung, Sterilisierung, Verpackung, Bereitstellung von Informationen durch den Hersteller und für Prüfverfahren fest.

Implants chirurgicaux non actifs - Implants de remplacement d'articulation - Exigences spécifiques relatives aux implants de remplacement de l'articulation du genou (ISO 21536:2007)

Neaktivni kirurški vsadki (implantati) - Sklepne proteze - Posebne zahteve za kolenske proteze (ISO 21536:2007)

General Information

Status
Withdrawn
Publication Date
14-Sep-2007
Withdrawal Date
05-May-2009
ICS
11.040.40 - Implants for surgery, prosthetics and orthotics
Technical Committee
CEN/TC 285 - Non-active surgical implants
Drafting Committee
CEN/TC 285/WG 4 - Joint replacement and tools and accessories
Current Stage
9960 - Withdrawal effective - Withdrawal
Start Date
06-May-2009
Completion Date
06-May-2009
Directive
93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
Mandate
M/023 - Standardization mandate to CEN/CENELEC concerning the development of European standards relating to medical devices
Ref Project
SIST EN ISO 21536:2008 - Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO 21536:2007)

Relations

Replaces
EN 12564:1998 - Non-active surgical implants - Joint replacement implants - Specific requirements for knee joint replacement implants
Effective Date
22-Dec-2008
Replaced By
EN ISO 21536:2009 - Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO 21536:2007)
Effective Date
13-May-2009

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 21536:2008
01-april-2008
1DGRPHãþD
SIST EN 12564:2000
Neaktivni kirurški vsadki (implantati) - Sklepne proteze - Posebne zahteve za
kolenske proteze (ISO 21536:2007)
Non-active surgical implants - Joint replacement implants - Specific requirements for
knee-joint replacement implants (ISO 21536:2007)
Nichtaktive chirurgische Implantate - Implantate zum Gelenkersatz - Besondere
Anforderungen an Implante für den Kniegelenkersatz (ISO 21536:2007)
Implants chirurgicaux non actifs - Implants de remplacement d'articulation - Exigences
spécifiques relatives aux implants de remplacement de l'articulation du genou (ISO
21536:2007)
Ta slovenski standard je istoveten z: EN ISO 21536:2007
ICS:
11.040.40
SIST EN ISO 21536:2008 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------

EUROPEAN STANDARD
EN ISO 21536
NORME EUROPÉENNE
EUROPÄISCHE NORM
September 2007
ICS 11.040.40 Supersedes EN 12564:1998
English Version
Non-active surgical implants - Joint replacement implants -
Specific requirements for knee-joint replacement implants (ISO
21536:2007)
Implants chirurgicaux non actifs - Implants de Nichtaktive chirurgische Implantate - Implantate zum
remplacement d'articulation - Exigences spécifiques Gelenkersatz - Besondere Anforderungen an Implantate für
relatives aux implants de remplacement de l'articulation du den Kniegelenkersatz (ISO 21536:2007)
genou (ISO 21536:2007)
This European Standard was approved by CEN on 16 August 2007.
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 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 Management Centre has the same status as the
official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland,
France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal,
Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: rue de Stassart, 36  B-1050 Brussels
© 2007 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 21536:2007: E
worldwide for CEN national Members.

---------------------- Page: 2 ----------------------

EN ISO 21536:2007 (E)
Contents Page
Foreword.3

2

---------------------- Page: 3 ----------------------

EN ISO 21536:2007 (E)
Foreword
This document (EN ISO 21536:2007) 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 March 2008, and conflicting national standards shall be withdrawn at
the latest by March 2008.
This document supersedes EN 12564:1998.
This document has been prepared under a mandate given to CEN by the European Commission and the
European Free Trade Association, and supports essential requirements of EC Directive(s).
For relationship with EC Directive(s), see informative Annex ZA which is an integral part of this document.
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, Cyprus, Czech
Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia,
Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain,
Sweden, Switzerland and the United Kingdom.
Endorsement notice
The text of ISO 21536:2007 has been approved by CEN as a EN ISO 21536:2007 without any modification.
3

---------------------- Page: 4 ----------------------

EN ISO 21536:2007 (E)

Annex ZA
(informative)

Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC


This European Standard has been prepared under a mandate given to CEN by the European Commission
and the Europ
...

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