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

Finish!
Privacy Policy

This is embarrasing...

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

CEN - EN ISO 10993-11

Biological evaluation of medical devices - Part 11: Tests for systemic toxicity

active, Most Current
Organization: CEN
Publication Date: 1 May 2018
Status: active
Page Count: 46
ICS Code (Biological evaluation of medical devices): 11.100.20
scope:

This document specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.

Document History

EN ISO 10993-11
May 1, 2018
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
This document specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
April 1, 2009
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
This part of ISO 10993 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
August 1, 2006
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
A description is not available for this item.
January 1, 1995
Biological Evaluation of Medical Devices - Part 11: Tests for Systemic Toxicity
A description is not available for this item.

References

Advertisement