MAUDE (Manufacturer and User Facility Device Experience) - Data Catalog 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
FDA Device Reports - ECRI Search FDA's Manufacturer and User Facility Device Experience (MAUDE) database
Searching MAUDE – Nested Knowledge This document describes how to retrieve medical device reports from the U S FDA’s Manufacturer and User Facility Device Experience (MAUDE) database in Nested Knowledge
FDA Manufacturer and User Facility Device Experience | NBER The FDA offers an Manufacturer and User Facility Device Experience (MAUDE) searchable database The Manufacturer and User Facility Device Experience consists of the four record types: Master Event, Device, Patient, and Text data files