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1. www.accessdata.fda.gov › cfdocs › cfmaudeManufacturer and User Facility Device Experience (MAUDE) Database

   www.accessdata.fda.gov › cfdocs › cfmaude

   • En caché

   Hace 6 días · 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...

2. www.accessdata.fda.gov › cfMAUDE › SearchManufacturer and User Facility Device Experience (MAUDE) Database

   www.accessdata.fda.gov › cfMAUDE › Search

   • En caché

   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...

3. open.fda.gov › data › maudeManufacturer and User Facility Device Experience

   open.fda.gov › data › maude

   • En caché

   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...

4. www.fda.gov › medical-devices › medical-deviceInformes de dispositivos médicos (MDR): Cómo informar de ...

   www.fda.gov › medical-devices › medical-device

   • En caché

   27 de jul. de 2023 · La FDA revisa todos los informes de dispositivos médicos (MDR) recibidos. El análisis del MDR de la FDA evalúa la totalidad de la información proporcionada en el MDR inicial, así como cualquier...

5. www.fda.gov › medical-devices › medical-deviceAdverse Event Reporting Data Files | FDA

   www.fda.gov › medical-devices › medical-device

   • En caché

   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.