UNLIMITED FREE ACCESS TO THE WORLD'S BEST IDEAS

close
Already an Engineering360 user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your Engineering360 Experience

close

Select Your Free Newsletters

Industry Newsletters

Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Standards Library
  • All
  • News & Analysis
  • Products & Services
  • Standards Library
  • Reference Library
  • Community

I forgot my password.

Don't have an account?

Register here.

ISO 22442-2

Medical devices utilizing animal tissues and their derivatives — Part 2: Controls on sourcing, collection and handling

inactive
Buy Now
Organization: ISO
Publication Date: 15 December 2007
Status: inactive
Page Count: 24
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

ISO 22442-2
September 1, 2020
Medical devices utilizing animal tissues and their derivatives — Part 2: Controls on sourcing, collection and handling
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...
ISO 22442-2
November 1, 2015
Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling
This part of ISO 22442 specifies requirements for controls on the sourcing, collection, and handling (which includes storage and transport) of animals and tissues for the manufacture of medical...
ISO 22442-2
December 15, 2007
Medical devices utilizing animal tissues and their derivatives — Part 2: Controls on sourcing, collection and handling
A description is not available for this item.

References

This document is referenced by:
AAMI 14971 - Medical devices— Application of risk management to medical devices
Published by AAMI on January 1, 2019
This document specifies terminology, principles and a process for risk management of medical devices, including software as a medical device and in vitro diagnostic medical devices. The process...
This document is referenced by:
ISO 14160 - Sterilization of health care products — Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives — Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
Published by ISO on September 1, 2020
This document specifies requirements for the characterization of a liquid chemical sterilizing agent and for the development, validation, process control and monitoring of sterilization by liquid...
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...
This document is referenced by:
SN EN ISO 15798/A1 - Ophthalmic implants - Ophthalmic viscosurgical devices; Amendment A1
Published by SNV on March 1, 2018
A description is not available for this item.
This document is referenced by:
AAMI 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 AAMI on January 1, 2006
This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices. NOTE Although the scope of this part of ISO...
View Less
View All
Advertisement