http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/search.CFM
"MAUDE data represents reports of adverse events involving medical devices. The data consists of voluntary reports since June 1993, user facility reports
since 1991, distributor reports since 1993, and manufacturer reports since August 1996. MAUDE may not include reports made according to exemptions, variances, or alternative reporting requirements granted under 21 CFR 803.19."
Who knew about this database?
Jonathan
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