ANSI/AAMI/ISO-13485 › 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)
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Document Number
ANSI/AAMI/ISO 13485:2016/(R)2019
Revision Level
2016 R19 EDITION
Status
Current
Publication Date
Jan. 1, 2019