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ANSI/AAMI/ISO 10993-11:2017/(R)2023

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

Summary

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. Annex 3

Technical characteristics

Publisher Association for the Advancement of Medical Instrumentation (AAMI)
Publication Date 01/01/2017
Confirmation Date 01/01/2023
Page Count 0
Themes Biological Evaluation
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