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FDA updates fields available in the Manufacturer and User Facility Device Experience (MAUDE) database and openFDA

Press releases may be edited for formatting or style | November 07, 2022 Health IT Risk Management
The U.S. Food and Drug Administration (FDA) updated its public adverse event databases to include fields for the Unique Device Identifier – Device Identifier (UDI-DI) and a modified version of the complete Unique Device Identifier (UDI-Public) in the search results.

The new fields are now available in the Manufacturer and User Facility Device Experience (MAUDE) database and the openFDA Device Adverse Event endpoint. This latest update is intended to ensure adverse event information in the databases is searchable.

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