UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

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

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

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

BSI - BS EN ISO 10993-2

Biological Evaluation of Medical Devices - Part 2: Animal Welfare Requirements

active, Most Current
Buy Now
Organization: BSI
Publication Date: 29 September 2006
Status: active
Page Count: 24
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

BS EN ISO 10993-2
November 30, 2022
Biological evaluation of medical devices Part 2: Animal welfare requirements
A description is not available for this item.
BS EN ISO 10993-2
November 30, 2022
Biological Evaluation of Medical Devices Part 2: Animal Welfare Requirements
A description is not available for this item.
BS EN ISO 10993-2
September 29, 2006
Biological Evaluation of Medical Devices - Part 2: Animal Welfare Requirements
A description is not available for this item.
BS EN ISO 10993-2
April 15, 1998
Biological Evaluation of Medical Devices - Part 2: Animal Welfare Requirements
A description is not available for this item.

References

This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the...
This document references:
ISO 10993-1 FRENCH - Évaluation biologique des dispositifs médicaux - Partie 1: Évaluation et essais au sein d'un processus de gestion du risque
Published by ISO on August 1, 2018
A description is not available for this item.
This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 10993-9 - Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products
Published by BSI on June 30, 2010
A description is not available for this item.
This document is referenced by:
BS EN ISO 10993-6 - Biological evaluation of medical devices Part 6: Tests for local effects after implantation
Published by BSI on December 31, 2016
A description is not available for this item.
View Less
View All

Related Products

Searching for related products...

Advertisement