Project No.EN ISO 10993-11:2018
TitleISO 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.
Registration number (WIID)60133
ScopeISO 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.
StatusStandarts spēkā
ICS group11.100.20