摘要
简要分析介绍新冠疫情下美国CDC的NPPTL所开展的非认证N95呼吸器PFE评估计划,为行业了解研究美国疫情中防护产品监管政策和检测工作的协同开展提供参考。
This paper briefly introduced and analyzed PFE assessment plan of non-NIOSH approved N95 respirators developed by NPPTL of CDC in response to the COVID-19 pandemic in the United States,to providing reference for the industry to understand the cooperation of American regulatory policy of personal protective equipments and related detecting action.
作者
张云
裴晓辉
周良彬
黄敏菊
ZHANG Yun;PEI Xiao-hui;ZHOU Liang-bin;HUANG Min-ju(Gongdong Medical Device Quality Surveillance and Test,Guangdong Guangzhou 510663;China Association for Medical Devices Industry,Beijing 100035)
出处
《中国医疗器械信息》
2021年第19期1-4,共4页
China Medical Device Information