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31 de may. 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
This database provides the most up-to-date list of voluntary...
- CLIA
Aquí nos gustaría mostrarte una descripción, pero el sitio...
- Adverse Events
The Manufacturer and User Facility Device Experience (MAUDE)...
- Download Files
The Manufacturer and User Facility Device Experience (MAUDE)...
- MDR Data Files Webpage
The FDA makes medical device reports available to patients...
- Cdrh FOIA Electronic Reading Room
Aquí nos gustaría mostrarte una descripción, pero el sitio...
- Post-Approval Studies
The FDA has the authority to require sponsors to perform a...
- De Novo
In 1997, the Food and Drug Administration Modernization Act...
- Standards
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...
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...
The MAUDE database houses medical device reports (MDRs) submitted to the FDA by mandatory reporters (manufacturers, importers and device user facilities) and voluntary reporters such as...
21 de jun. de 2019 · Information about the Adverse Event Reporting Data Files including Manufacturer and User Facility Device Experience (MAUDE) data and Medical Device Reporting (MDR) data.