ISO/DIS-13485 › Medical devices - Quality management systems - Requirements for regulatory purposes

ISO/DIS-13485 - 3RD EDITION FINAL DRAFT - SUPERSEDED -- See the following: ISO-13485
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Medical devices - Quality management systems - Requirements for regulatory purposes
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Medical devices. Quality management systems. Requirements for regulatory purposes

Document Number

ISO/FDIS 13485

Revision Level

3RD EDITION FINAL DRAFT

Status

Superseded

Publication Date

Oct. 29, 2015

Committee Number

ISO/TC 210