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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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   Há 6 dias · The MAUDE database contains reports of adverse events involving medical devices submitted to the FDA by mandatory and voluntary reporters. Users can search the database by product, event, date, manufacturer, etc.

   • 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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   The MAUDE database contains adverse event reports of medical devices submitted by manufacturers, importers, and user facilities. Learn about the database description, limitations, fields, and how to access the data.

3. www.accessdata.fda.gov › cfMAUDE › TextSearchMAUDE - Manufacturer and User Facility Device Experience

   www.accessdata.fda.gov › cfMAUDE › TextSearch

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   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...

4. 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 by manufacturers, importers, device user facilities and others. The FDA uses MAUDE to monitor device performance, detect safety issues and contribute to benefit-risk assessments.

5. 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,...