医疗器械不良事件报告覆盖范围窄，质量有待提高。
The scope that the reports covered is narrow and the quality needs to be raised.
针对辖区内医疗器械不良事件报告率低的现象，结合现行的监测管理模式，查找并分析原因。
Focusing on the phenomena that the reported adverse event of medical device is quite low, we use the method to analyze the cause on the base of actual monitoring management.
结果医疗器械安全质量通过医疗器械不良事件报告、医疗器械召回和医疗器械追踪得以实现。
Results Management of medical devices for safety and quality is to be achieved by means of reports of adverse events, recall and follow-up of medical devices.
目的通过对广东省2007年接收的可疑医疗器械不良事件报告表进行统计分析，为进一步开展监测工作提供参考。
Objective By analyzing the Medical Device Administration Events (MDAE) reports of Guangdong Province in 2007, to provide references for monitoring work.
开展医疗器械不良事件监测和报告工作是十分重要的。
It is important to carry out the work of monitoring and reporting the adverse events of medical instruments.
开展医疗器械不良事件监测和报告工作是十分重要的。
It is important to carry out the work of monitoring and reporting the adverse events of medical instruments.
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