BEUDAMED
    FDA Adverse Event Death Summary report: N

    2951413-2001-00001

    MDR report key: 349003 · Received August 23, 2001

    Report

    Report Number
    2951413-2001-00001
    Event Type
    Death
    Date Received
    August 23, 2001
    Date of Event
    July 20, 2001
    Product Code
    MAF
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    38535 MAF

    Patients

    Seq Age Sex Outcome Treatment
    1