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  1. Home
  2. DIN EN ISO 13485 Corrigendum 1

DIN EN ISO 13485 Corrigendum 1 Historical [ Withdrawn ]

1985611

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

Corrigenda by DIN-adopted European-adopted ISO Standard , 07/01/2017

This document has been replaced. View the most recent version.
This document is a corrigenda. View the base document.

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Document History

  1. DIN EN ISO 13485

    December 2021
    Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) (includes Corrigendum :2018)

    • Most Recent  Most Recent
  2. DIN EN ISO 13485/A1 - DRAFT

    November 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

    • Historical Version
  3. DIN EN ISO 13485 Corrigendum 1

    You are currently viewing this product 👀 currently
    viewing

    July 2017
    Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016) , Corrigendum to DIN EN ISO 13485:2016-08

    • Historical Version
  4. DIN EN ISO 13485

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

    • Historical Version
  5. DIN EN ISO 13485 - DRAFT

    May 2015
    Draft Document - Medical devices - Quality management systems - Requirements for regulatory purposes (ISO/DIS 13485:2015); German and English version prEN ISO 13485:2015

    • Historical Version
  6. DIN EN ISO 13485 - DRAFT

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

    • Historical Version
  7. DIN EN ISO 13485

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

    • Historical Version
  8. DIN EN ISO 13485

    January 2010
    Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003 + Cor. 1:2009) (includes Corrigendum AC:2009)

    • Historical Version
  9. DIN EN ISO 13485

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

    • Historical Version

Browse related products from DIN-adopted European-adopted ISO Standard

  • Deutsches Institut Fur Normung E.V. (German National Standard) > By ICS Code > 11: Health Care Technology > 11.040: Medical equipment > 11.040.01: Medical equipment in general

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Published:

07/01/2017

Number of Pages:

20

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1 file

Product Code(s):

2805639, 2677030, 2805639, 2677030

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