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.
OBJAVLJEN
ISO 10993-11:2017
PROJEKAT
ISO/DIS 10993-11.2
40.00
Dopunjavanje i evidentiranje podataka o nacrtu standarda
17. 4. 2026.
Biološko vrednovanje medicinskih sredstava – Deo 11: Ispitivanja sistemske toksičnosti
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