DIN-EN-ISO-13485 Historical Revision Information
Medical devices - Quality management systems - Requirements for regulatory purposes

DIN-EN-ISO-13485 - 2016 EDITION CORRIGENDUM 1 - SUPERSEDED
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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

DIN EN ISO 13485 Berichtigung 1:2017-07

Revision Level

2016 EDITION CORRIGENDUM 1

Status

Superseded

Publication Date

July 1, 2017