This data package includes reports of adverse events involving medical devices actually, information on medical devices which may have malfunctioned or caused a death or serious injury during the years 1984 through 1996 and medical product safety network program data.
Access to weekly updated FDA Manufacturer And User Facility Device Experience (MAUDE) data.; Access to medical device reporting (MDR) data during the years 1984 through 1996.; Access to the Medical Product Safety Network (MedSun) data that involves the reporting of problems with medical products from a network of approximately 300 hospitals, nursing homes and home health facilities around the United States.
Update Frequency: Weekly/Never
1. Manufacturer And User Facility Device Experience Database
2. MAUDE with Patient Involvement
3. Medical Device Reporting
4. Medical Product Safety Network