Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2026)

prEN ISO 10993-11

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.

Abstract

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.

Info

Stage Date

2026-05-21

Stage Code

40.20.0000 - 40.20.0000

Sector

Health Sciences

Technical Committee

TE-T 14

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