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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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   31 de mai. 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 last...

   • Maude

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

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

   www.accessdata.fda.gov › cfMAUDE › TextSearch

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   31 de mai. 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 last...

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

   www.accessdata.fda.gov › cfMAUDE › Search

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   31 de mai. 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...

4. 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 Manufacturer and User Facility Device Experience (MAUDE) database contains medical device reports (MDRs) of adverse events. To further promote transparency, the...

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

   open.fda.gov › data › maude

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   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...

6. www.ncbi.nlm.nih.gov › books › NBK570582Use and Application Of MAUDE In Patient Safety - StatPearls ...

   www.ncbi.nlm.nih.gov › books › NBK570582

   24 de abr. de 2023 · The Manufacturer and User Facility Device Experience (MAUDE) database is an online searchable and publicly accessible repository developed by the United States Food and Drug Administration (FDA) for systematic data collection of adverse outcomes related to the medical devices.

7. www.fda.gov › medical-devices › medical-deviceMDR Data Files | FDA

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

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   18 de fev. de 2022 · The FDA makes medical device reports available to patients and health care providers on the FDA's public Manufacturer and User Facility Device Experience (MAUDE) database as one source of...