摘要
医疗器械的无菌屏障系统是无菌医疗器械安全性的基本保证,本文从包装材料的微生物屏障、生物相容性和毒理学特性、物理和化学特性、与成型或密封过程的适应性、与预期灭菌过程的适应性、与标签系统的适应性等方面,阐述最终灭菌医疗器械包装材料的选择。
The sterile barrier system is the basic protection of the safety of sterilized medical devices.This paper focuses on the material choice for terminally sterilize medical devices from a number of aspects including microbial barrier,biocompatibility and toxicological attributes,physical and chemical properties,compatibility with respect to forming and sealing processes,compatibility with respect to the intended sterilization processes,and compatibility with respect to label system.
出处
《中国医疗器械信息》
2011年第8期14-15,34,共3页
China Medical Device Information
关键词
无菌
材料
选择
sterilization
materials
choice
