Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants - Amendment 1 (ISO 21536:2007/Amd 1:2014)

2012-09-18 GVN: Draft for // vote received at ISO/CS (see notification in dataservice on 2012-09-18)

Nichtaktive chirurgische Implantate - Implantate zum Gelenkersatz - Besondere Anforderungen an Implantate für den Kniegelenkersatz - Änderung 1 (ISO 21536:2007/Amd 1:2014)

N/A

Implants chirurgicaux non actifs - Implants de remplacement d'articulation - Exigences spécifiques relatives aux implants de remplacement de l'articulation du genou - Amendement 1 (ISO 21536:2007/Amd 1:2014)

Neaktivni kirurški vsadki (implantati) - Sklepne proteze - Posebne zahteve za kolenske proteze - Dopolnilo A1 (ISO 21536:2007/Amd 1:2014)

Ta mednarodni standard navaja posebne zahteve za kolenske proteze. V zvezi z varnostjo ta mednarodni standard določa zahteve za predvidene lastnosti, obliko, materiale, vrednotenje oblike, izdelavo, sterilizacijo, pakiranje in informacije, ki jih zagotovi proizvajalec, ter preskusne metode.

General Information

Status
Published
Publication Date
04-Mar-2014
Withdrawal Date
29-Sep-2014
Current Stage
6060 - Definitive text made available (DAV) - Publishing
Start Date
05-Mar-2014
Completion Date
05-Mar-2014

Relations

Buy Standard

Amendment
EN ISO 21536:2009/A1:2014
English language
8 pages
sale 10% off
Preview
sale 10% off
Preview
e-Library read for
1 day

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 21536:2009/A1:2014
01-maj-2014
Neaktivni kirurški vsadki (implantati) - Sklepne proteze - Posebne zahteve za
kolenske proteze - Dopolnilo A1 (ISO 21536:2007/Amd 1:2014)
Non-active surgical implants - Joint replacement implants - Specific requirements for
knee-joint replacement implants - Amendment 1 (ISO 21536:2007/Amd 1:2014)
Nichtaktive chirurgische Implantate - Implantate zum Gelenkersatz - Besondere
Anforderungen an Implantate für den Kniegelenkersatz - Änderung 1 (ISO
21536:2007/Amd 1:2014)
Implants chirurgicaux non actifs - Implants de remplacement d'articulation - Exigences
spécifiques relatives aux implants de remplacement de l'articulation du genou -
Amendement 1 (ISO 21536:2007/Amd 1:2014)
Ta slovenski standard je istoveten z: EN ISO 21536:2009/A1:2014
ICS:
11.040.40 Implantanti za kirurgijo, Implants for surgery,
protetiko in ortetiko prosthetics and orthotics
SIST EN ISO 21536:2009/A1:2014 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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

SIST EN ISO 21536:2009/A1:2014

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

SIST EN ISO 21536:2009/A1:2014

EUROPEAN STANDARD
EN ISO 21536:2009/A1

NORME EUROPÉENNE

EUROPÄISCHE NORM
March 2014
ICS 11.040.40
English Version
Non-active surgical implants - Joint replacement implants -
Specific requirements for knee-joint replacement implants -
Amendment 1 (ISO 21536:2007/Amd 1:2014)
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 - Änderung 1 (ISO 21536:2007/Amd
genou - Amendement 1 (ISO 21536:2007/Amd 1:2014) 1:2014)
This amendment A1 modifies the European Standard EN ISO 21536:2009; it was approved by CEN on 4 January 2014.

CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for inclusion of this
amendment into the relevant 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 amendment 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, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania,
Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, 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: Avenue Marnix 17, B-1000 Brussels
© 2014 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 21536:2009/A1:2014 E
worldwide for CEN national Members.

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

SIST EN ISO 21536:2009/A1:2014
EN ISO 21536:2009/A1:2014 (E)
Contents Page
Foreword .3
Annex ZA (informative) Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC on medical devices .4
2

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

SIST EN ISO 21536:2009/A1:2014
EN ISO 21536:2009/A1:2014 (E)
Foreword
This document (EN ISO 21536:2009/A1:2014) has been prepared by Technical Committee ISO/TC 150
"Implants for surgery" in collaboration Technical Committee CEN/TC 285 “Non-active surgical implants” the
secretariat of which is held by DIN.
This Amendment to the European Standard EN ISO 21536:2009 shall be given the status of a national
standard, either by publication of an identical text or by endorsement, at the latest by September 2014, and
conflicting national standards shall be withdrawn at the latest by September 2014.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent rights.
This document has been prepared under a mandate given to CEN by the European Commission and the
European Free Trade Association, and supports essential r
...

Questions, Comments and Discussion

Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.