FDA
收藏国家生物信息中心2025-10-11 更新2025-03-15 收录
下载链接：
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/search
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资源简介：
he FDA requires that manufacturers and device users submit medical device reports (MDRs) for suspected injuries from device use or malfunction. The database of MDRs, entitled Manufacturer and User Facility Device Experience (MAUDE) enables the FDA to monitor device performance and identify potential safety issues.
提供机构：
Massachusetts General Hospital
创建时间：
2018-01-28
