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EEC - EC REGULATION NO 722

COMMISSION REGULATION concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin

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Organization: EEC
Publication Date: 8 August 2012
Status: active
Page Count: 10

Document History

EC REGULATION NO 722
August 8, 2012
COMMISSION REGULATION concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin
A description is not available for this item.

References

This document is referenced by:
ISO 22442-2 - Medical devices utilizing animal tissues and their derivatives — Part 2: Controls on sourcing, collection and handling
Published by ISO on September 1, 2020
This document specifies requirements for controls on the sourcing, collection, and handling (which includes storage and transport) of animals and tissues for the manufacture of medical devices...
This document is referenced by:
EN ISO 22442-2 - Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling
Published by CEN on December 1, 2020
This document specifies requirements for controls on the sourcing, collection, and handling (which includes storage and transport) of animals and tissues for the manufacture of medical devices...
This document is referenced by:
DIN EN ISO 22442-2 - Tierische Gewebe und deren Derivate, die zur Herstellung von Medizinprodukten eingesetzt werden - Teil 2: Kontrollen der Beschaffung, Materialgewinnung und Handhabung (ISO 22442-2:2020); Deutsche Fassung EN ISO 22442-2:2020
Published by DIN on April 1, 2021
A description is not available for this item.
This document is referenced by:
IPC-6012 - Medical Applications Addendum to IPC-6012E, Qualification and Performance Specification for Rigid Printed Boards
Published by IPC on August 1, 2020
This Specification covers qualification and performance requirements of Rigid Printed Board for Medical Device Applications. The Printed Boards may have a design that contains HDI and Design Level D...
This document is referenced by:
SN EN ISO 22442-2 - Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling
Published by SNV on April 1, 2021
This document specifies requirements for controls on the sourcing, collection, and handling (which includes storage and transport) of animals and tissues for the manufacture of medical devices...
This document is referenced by:
IPC-6013 - Qualification and Performance Specification for Flexible and Rigid-Flexible Printed Boards
Published by IPC on April 1, 2018
A description is not available for this item.
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