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30 de abr. 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
The Manufacturer and User Facility Device Experience (MAUDE)...
- Download Files
The FDA uploads these into the MAUDE database and includes...
- MDR Data Files Webpage
Like all MDR data in MAUDE, MDR data in ASR reports cannot...
- FDA Guidance Documents
Some FDA guidance documents on this list are indicated as...
- Post-Approval Studies
Mandated Studies Program Food and Drug Administration 10903...
- De Novo
In 1997, the Food and Drug Administration Modernization Act...
- Standards
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23 de oct. de 2023 · Manufacturer and User Facility Device Experience (MAUDE) database represents reports of adverse events involving medical devices. The searchable database contains the last 10 years of medical ...
30 de abr. de 2024 · The MAUDE database houses medical device reports submitted to the FDA by mandatory reporters 1 (manufacturers, importers and device user facilities) and voluntary reporters such as health care...
