SS ISO 10993-11:2017

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

OVERVIEW

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.

Potential users of the standards on biological evaluation of medical devices may include companies expanding into medical technology, medical technology start-ups, research institutes and institutes for higher learning.

COMMENTS

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PRODUCT DETAILS

Status Current
Edition 2017
No. of Pages 41
ICS Classification 11.100.20 Biological evaluation of medical devices
Committee Biomedical and Health Standards Committee
Available for Purchase Global
Adoption ISO 10993-11 : 2017 IDT