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.

- Trained on our vast library of engineering resources.

AAMI 10993-11

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

active, Most Current
Buy Now
Organization: AAMI
Publication Date: 1 January 2017
Status: active
Page Count: 38
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

January 1, 2017
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.
AAMI 10993-11
January 1, 2017
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.
January 1, 2006
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
Specifies requirements and gives guidance on the procedures to be followed in the evaluation of the potential for medical devices and their materials to cause adverse systemic reactions.
January 1, 2006
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.
January 1, 2006
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.
January 1, 1993
BIOLOGICAL EVALUATION OF MEDICAL DEVICES, PART 11: TESTS FOR SYSTEMIC TOXICITY
A description is not available for this item.

References

Advertisement