AAMI - 10993-11
Biological evaluation of medical devices—Part 11: Tests for systemic toxicity
inactive
| Organization: | AAMI |
| Publication Date: | 1 January 2006 |
| Status: | inactive |
| Page Count: | 39 |
scope:
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.
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.
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.
10993-11
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.
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