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.
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
Query capabilities
Search fields
facility_nameprice_referencefacility_idFilter fields
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