More Info

MAUDE – Manufacturer and User Facility Device Experience DatabaseRestricted to faculty, students, and staff at The University of Missouri

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. From the FDA Center for Devices & Radiological Health.

Date Coverage: 1993-


Search Guide: http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/help.cfm

Auto Alerts: http://libraryguides.missouri.edu/content.php?pid=92982&sid=1474480#maude