数据库简述：Food and Drug Administration
数据库主要信息：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.
Massachusetts General Hospital
Department of Dermatology and Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts
Contact name (PI/Team):
Anne Marie Tremaine MD
Contact email (PI/Helpdesk):