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NEN-EN-ISO 21536/A1

Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants

active, Most Current
Organization: NEN
Publication Date: 1 March 2014
Status: active
Page Count: 14
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

NEN-EN-ISO 21536/A1
March 1, 2014
Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
A description is not available for this item.
NEN-EN-ISO 21536/A1
March 1, 2012
Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
A description is not available for this item.
NEN-EN-ISO 21536
May 2, 2009
Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
This International Standard provides specific requirements for knee joint replacement implants. With regard to safety, this International Standard specifies requirements for intended performance,...
NEN-EN-ISO 21536
October 1, 2007
Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
This International Standard provides specific requirements for knee joint replacement implants. With regard to safety, this International Standard specifies requirements for intended performance,...
NEN-EN-ISO 21536
April 1, 2006
Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
This International Standard provides specific requirements for knee joint replacement implants. With regard to safety, this International Standard specifies requirements for intended performance,...

References

This document references:
2007/47/EG - Richtlijn 2007/47/EG van het Europees Parlement en de Raad van 5 september 2007 tot wijziging van Richtlijn 90/385/EEG van de Raad betreffende de onderlinge aanpassing van de wetgevingen van de lidstaten inzake actieve implanteerbare medische hulpmiddelen, Richtlijn 93/42/EEG van de Raad betreffende medische hulpmiddelen en Richtlijn 98/8/EG betreffende het op de markt brengen van biociden
Published by NEN on September 5, 2007
Council Directive 93/42/EEC (3) requires the Commission to submit a report to the Council, no later than five years from the date of implementation of that Directive, concerning: (i) information on...
This document references:
93/42/EEG - Richtlijn 93/42/EEG van de Raad van 14 juni 1993 betreffende medische hulpmiddelen
Published by NEN on July 12, 1993
A description is not available for this item.
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