United States·health

US openFDA — Medical device adverse events (MAUDE)

FDA MAUDE database of medical device adverse event reports: report number, device brand and generic name, event type, and report dates. Aggregate public data from openFDA — not patient records.

us_openfda_device_adverse_events15,000,000 recordsCachedCached endpoint

About this product

FDA MAUDE database of medical device adverse event reports: report number, device brand and generic name, event type, and report dates. Aggregate public data from openFDA — not patient records.

Record count
15,000,000 records
Source type
Cached endpoint
Last refreshed
Refresh cadence not published
Group
Healthcare Regulatory

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