摘要
简单介绍灭菌的基础理论、医疗器械环氧乙烷灭菌的特点和影响灭菌效果的关键因素,并分析比较了医疗器械环氧乙烷灭菌的产品放行所使用的无菌检查法、传统放行和参数放行三种方法,着重研究了参数放行的理论基础、可行性、确认要求及优缺点。
This study briefly introduces the basic theory of sterilization,the characteristics of ethylene oxide sterilization for medical devices and the key factors about sterilization effectiveness,analyzes and compares three methods used in the product release of medical devices sterilized by ethylene oxide:test for sterility,traditional release and parametric release,and focuses on the theoretical basis,feasibility,validation requirements,advantages and disadvantages of parametric release.
作者
黄鸿新
胡昌明
刘文一
崔文波
徐海英
祝沛平
HUANG Hongxin;HU Changming;LIU Wenyi;CUI Wenbo;XU Haiying;ZHU Peiping(Guangdong Medical Devices Quality Surveillance and Test Institute,Guangzhou,510663;Suzhou GOLAS Medical Technology Co.Ltd.,Suzhou,215000;Xinxiang Huaxi Sanitary Materials Co.Ltd.,Xinxiang,453412;Suzhou Prosteri Medical Technology Co.Ltd.,Suzhou,215000)
出处
《中国医疗器械杂志》
2022年第5期574-577,共4页
Chinese Journal of Medical Instrumentation
关键词
无菌保证水平
灭菌过程参数
参数放行
sterility assurance level
sterilization process parameters
parametric release