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ISO 22442-2 FRENCH

Dispositifs médicaux utilisant des tissus animaux et leurs dérivés — Partie 2: Contrôles de l'origine, de la collecte et du traitement

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Organization: ISO
Publication Date: 1 September 2020
Status: active
Page Count: 24
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

ISO 22442-2 FRENCH
September 1, 2020
Dispositifs médicaux utilisant des tissus animaux et leurs dérivés — Partie 2: Contrôles de l'origine, de la collecte et du traitement
A description is not available for this item.
ISO 22442-2 FRENCH
November 1, 2015
Dispositifs médicaux utilisant des tissus animaux et leurs dérivés - Partie 2: Contrôles de l’origine, de la collecte et du traitement
A description is not available for this item.
ISO 22442-2 FRENCH
December 15, 2007
Dispositifs médicaux utilisant des tissus animaux et leurs dérivés - Partie 2: Contrôles de l'origine, de la collecte et du traitement
A description is not available for this item.

References

This document is referenced by:
BS EN ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by BSI on September 29, 2006
A description is not available for this item.
This document is referenced by:
BS PD ISO/TS 10993-19 - Biological evaluation of medical devices Part 19: Physico-chemical, morphological and topographical characterization of materials
Published by BSI on March 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 11137-1 - Sterilization of health care products — Radiation Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
Published by BSI on July 31, 2015
A description is not available for this item.
This document is referenced by:
BS EN ISO 13408-5 - Aseptic processing of health care products Part 5: Sterilization in place
Published by BSI on October 30, 2011
A description is not available for this item.
This document is referenced by:
ISO 18362 - Manufacture of cell-based health care products - Control of microbial risks during processing
Published by ISO on February 1, 2016
This International Standard specifies the minimum requirements for, and provides guidance on, a risk-based approach for the processing of cell-based health care products (CBHPs) requiring control of...
This document is referenced by:
ISO 13022 - Medical products containing viable human cells - Application of risk management and requirements for processing practices
Published by ISO on April 1, 2012
This International Standard specifies requirements and guidance for processing practices and managing risk associated with viable cellular components of products regulated as medicinal products,...
This document is referenced by:
ISO TR 22442-4 - Medical devices utilizing animal tissues and their derivatives — Part 4: Principles for elimination and/or inactivation of transmissible spongiform encephalopathy (TSE) agents and validation assays for those processes
Published by ISO on December 1, 2010
This Technical Report offers suggestions for designing and conducting validation assays to help determine if processes used in the manufacture of medical devices derived from non-viable animal...
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