MAUDE (Manufacturer and User Facility Device Experience)

Description

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.

Resources

Name Format Description Link
21 search.CFM http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/search.CFM

Tags

  • cdrh

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