DIN-EN-ISO-13485 › Historical Revision Information
Medical devices - Quality management systems - Requirements for regulatory purposes
Medical devices - Quality management systems - Requirements for regulatory purposes
To find similar documents by classification:
03.120.10 (Quality management and quality assurance)
11.040.01 (Medical equipment in general)
This document comes with our free Notification Service, good for the life of the document.
This document is available in either Paper or PDF format.
Document Number
DIN EN ISO 13485:2007-10
Revision Level
2007 EDITION
Status
Superseded
Publication Date
Oct. 1, 2007