DIN EN ISO 13485 Corrigendum 1 PDF

Published Date: 12/01/2021

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) (includes Corrigendum :2018)

Published Date: 11/01/2019

Draft Document - Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German and English version EN ISO 13485:2016/prA1:2019

Published Date: 07/01/2017

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) , Corrigendum to DIN EN ISO 13485:2016-08

Published Date: 04/01/2014

Draft Document - Medical devices - Quality management systems - Requirements for regulatory purposes (ISO/DIS 13485:2014); German version prEN ISO 13485:2014

Published Date: 11/01/2012

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003 + Cor. 1:2009) (includes Corrigendum :2012)

Published Date: 01/01/2010

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003 + Cor. 1:2009) (includes Corrigendum AC:2009)

Published Date: 10/01/2007

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003) (includes Corrigendum AC:2007)

Published Date: 10/01/2024

Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers (IEC 60601-2-21:2020 + AMD1:2023); German version EN IEC 60601-2-21:2021 + A1:2023

Published Date: 03/01/2022

Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021, Corrected version 2021-12)

Published Date: 02/01/2022

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021)

Published Date: 05/01/2000

Published Date: 01/01/1996

Published Date: 01/01/1996

Published Date: 08/01/1997