ISO-10993-11 › Biological evaluation of medical devices - Part 11: Tests for systemic toxicity

ISO-10993-11 - 3RD EDITION - CURRENT
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ISO 10993-11:2017 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.

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11.100.20 (Biological evaluation of medical devices Medical microbiology, see 07.100.10)

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ISO-10993-1
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process

Document Number

ISO 10993-11:2017

Revision Level

3RD EDITION

Status

Current

Publication Date

Sept. 1, 2017

Committee Number

ISO/TC 194