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ISO 13485 FRENCH

Medical devices Quality management systems Requirements for regulatory purposes

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Organization: ISO
Publication Date: 15 July 2003
Status: inactive
Page Count: 70
ICS Code (Quality management and quality assurance): 03.120.10
ICS Code (Medical equipment in general): 11.040.01

Document History

ISO 13485 FRENCH
March 1, 2016
Medical devices Quality management systems Requirements for regulatory purposes
A description is not available for this item.
ISO 13485 FRENCH
August 1, 2009
Medical devices — Quality management systems — Requirements for regulatory purposes — TECHNICAL CORRIGENDUM 1
A description is not available for this item.
ISO 13485 FRENCH
July 15, 2003
Medical devices Quality management systems Requirements for regulatory purposes
A description is not available for this item.

References

This document is referenced by:
BS EN ISO 14937 - Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
Published by BSI on March 31, 2010
A description is not available for this item.
This document is referenced by:
BS EN 556-1 - Sterilization of Medical Devices - Requirements for Medical Devices to Be Designated "Sterile" - Part 1: Requirements for Terminally Sterilized Medical Devices
Published by BSI on December 11, 2001
A description is not available for this item.
This document is referenced by:
BS EN 60601-1-6 + A2 - Medical electrical equipment Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability
Published by BSI on May 31, 2010
A description is not available for this item.
This document is referenced by:
BS EN ISO 14971 + A11 - Medical devices - Application of risk management to medical devices
Published by BSI on December 31, 2019
A description is not available for this item.
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