AENOR - UNE-EN ISO 13485
Medical devices - Quality management systems - Requirements for regulatory purposes - Technical Corrigendum 1 (ISO 13485:2003+Cor 1:2009)
inactive
| Organization: | AENOR |
| Publication Date: | 29 May 2013 |
| Status: | inactive |
| Page Count: | 86 |
| ICS Code (Medical equipment in general): | 11.040.01 |
| ICS Code (Management systems): | 03.100.70 |
Document History
September 21, 2022
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
A description is not available for this item.
July 25, 2018
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016). (Consolidated version)
A description is not available for this item.
April 12, 2017
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
A description is not available for this item.
May 25, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
A description is not available for this item.
UNE-EN ISO 13485
May 29, 2013
Medical devices - Quality management systems - Requirements for regulatory purposes - Technical Corrigendum 1 (ISO 13485:2003+Cor 1:2009)
A description is not available for this item.
May 23, 2012
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)
A description is not available for this item.
October 21, 2009
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003/Cor 1:2009)
A description is not available for this item.
October 31, 2007
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)
A description is not available for this item.
June 25, 2004
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)
A description is not available for this item.
March 12, 2004
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)
A description is not available for this item.
July 20, 2001
Quality systems - Medical devices - Particular requirements for the application of EN ISO 9001. (ISO 13485:1996)
A description is not available for this item.