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Aug 31, 2024 · The Manufacturer and User Facility Device Experience (MAUDE) database is a searchable database of medical device reports (MDRs) of adverse events involving medical devices over the last...
Description of the MAUDE Database. The Manufacturer and User Facility Device Experience (MAUDE) database contains medical device reports (MDRs) of adverse events.
The MAUDE database houses medical device reports (MDRs) submitted to the FDA by mandatory reporters (manufacturers, importers and device user facilities) and voluntary reporters such as...
Jun 21, 2019 · Information about the Adverse Event Reporting Data Files including Manufacturer and User Facility Device Experience (MAUDE) data and Medical Device Reporting (MDR) data.
Jun 12, 2024 · These medical device reports have been available in the FDA's public Manufacturer and User Facility Device Experience (MAUDE) database since 1999 as one source of information to help patients...
Apr 24, 2023 · The Manufacturer and User Facility Device Experience (MAUDE) database is an online searchable and publicly accessible repository developed by the United States Food and Drug Administration (FDA) for systematic data collection of adverse outcomes related to the medical devices.
The Maude Database, short for Manufacturer and User Facility Device Experience, is a publicly accessible database maintained by the U.S. Food and Drug Administration (FDA). It serves as a repository for reports of adverse events and product problems associated with medical devices.
