DIN Standards Committee Optics and Precision Mechanics
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
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.
Begin
2023-04-19
WI
00206098
Planned document number
prEN ISO 10993-11 rev
Responsible national committee
NA 027-07-12 AA - Biological evaluation of medical devices
Responsible european committee
CEN/TC 206 - Biological and clinical evaluation of medical devices
previous edition(s)
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)
2018-05
