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31 de jul. de 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...
- Standards
Medical Device Reports (MAUDE) CDRH Export Certificate...
- CLIA
Aquí nos gustaría mostrarte una descripción, pero el sitio...
- Adverse Events
Conducting searches in the MAUDE Database: The Manufacturer...
- Download Files
The FDA uploads these into the MAUDE database and includes...
- MDR Data Files Webpage
MAUDE Data Downloadable Files. This section provides...
- MedSun Reports
The Medical Product Safety Network (MedSun) is an adverse...
- Radiation-Emitting Electronic Products Corrective Actions
This database includes: electronic products for which...
- Postmarket Surveillance Studies
The FDA has the authority to require device manufacturers to...
- Standards
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