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

   www.accessdata.fda.gov › cfdocs › cfmaude

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   30 de abr. de 2024 · MAUDE is a searchable database of adverse events involving medical devices over the last ten years. Users can search on product, problem, event type, manufacturer, model number, report number and other fields to find reports submitted by mandatory or voluntary reporters.

   • Maude

     The MAUDE database houses medical device reports submitted...

   • Standards

     This database provides the most up-to-date list of voluntary...

   • CLIA

     Gostaríamos de exibir a descriçãoaqui, mas o site que você...

   • Adverse Events

     The Manufacturer and User Facility Device Experience (MAUDE)...

2. www.fda.gov › medical-devices › mandatory-reportingAbout Manufacturer and User Facility Device Experience (MAUDE)

   www.fda.gov › medical-devices › mandatory-reporting

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   23 de out. de 2023 · MAUDE (Manufacturer and User Facility Device Experience) contains reports of adverse events involving medical devices. The database is searchable by the public and provides data files for downloading since 1991.

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

   open.fda.gov › data › maude

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   MAUDE contains reports of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by mandatory and voluntary reporters. Learn about the data sources, limitations, and how to access the database.

4. www.fda.gov › medical-devices › medical-device-safetyMedical Device Reporting (MDR): How to Report Medical Device ...

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

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   27 de jul. de 2023 · The MAUDE database houses MDRs submitted to the FDA by mandatory reporters (manufacturers, importers and device user facilities) and voluntary reporters such as health care professionals, patients ...

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

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

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   21 de jun. de 2019 · The FDA provides data files of adverse events involving medical devices reported by manufacturers, distributors, and user facilities. The data include MAUDE, DEN, and ASR data from 1984 to 2019.