MAUDE (Manufacturer and User Facility Device Experience)
MAUDE data represents reports of adverse events involving medical devices. The data consists of all voluntary reports since June, 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August, 1996.
Complete Metadata
| bureauCode |
[ "009:10" ] |
|---|---|
| identifier | 1327f116-da9f-40b9-babd-c893ab2ceacd |
| issued | 2021-02-25 |
| landingPage | http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/search.CFM |
| programCode |
[ "009:005" ] |
| references |
[ "http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/PostmarketRequirements/ReportingAdverseEvents/ucm127891.htm" ] |
| temporal | 1991-01-01/2013-10-31 |
| theme |
[ "FDA" ] |
