Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
医疗器械生物学评价 第11部分:全身毒性试验
发布日期:
2017-09-14
ISO 10993-11:2017规定了在评估医疗器械材料引起不良全身反应的可能性时应遵循的要求和程序指南。
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.