Publikuar
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.
WITHDRAWN
ISO 10993-11:2006
PUBLISHED
ISO 10993-11:2017
90.92
Standard to be revised
18 pri 2023
IN_DEVELOPMENT
ISO/CD 10993-11
Vlerësimi biologjik i pajisjeve mjekësore - Pjesa 11: Testet për toksicitetin sistemik (ISO 10993-11:2017)
60.60 Standard published