摘要
本文探讨从植入医疗器械临床使用和手术后各环节的不良事件跟踪,加强对植入医疗器械的监督管理,最终保证医疗器械在人体内使用的安全有效性。
Discusses the causes of adverse events in the clinical use of implantable medical instruments and after operations. And puts forward the importance of the adverse event monitoring for implantable medical instruments so as to ensure the safety and effectiveness of medical instruments used in the human body.
出处
《中国医疗设备》
2008年第12期64-66,共3页
China Medical Devices
关键词
植入医疗耗材
植入物管理
不良事件监测
implantable medical consumable
implants management
adverse event monitoring
