Projekta Nr.prEN ISO 10993-11
NosaukumsISO 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.
Reģistrācijas numurs (WIID)77933
Darbības sfēraISO 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.
StatussAptauja slēgta
ICS grupa11.100.20