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  1. 30 de jun. 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

      Medical Device Reports (MAUDE) CDRH Export Certificate...

    • CLIA

      Aquí nos gustaría mostrarte una descripción, pero el sitio...

    • Adverse Events

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

    • Download Files

      The FDA uploads these into the MAUDE database and includes...

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  4. 30 de jun. 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 care...

  5. 30 de jun. 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...

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