BEUDAMED
    FDA Adverse Event Death Summary report: N

    2242551-1998-00035

    MDR report key: 204583 · Received December 30, 1998

    Report

    Report Number
    2242551-1998-00035
    Event Type
    Death
    Date Received
    December 30, 1998
    Date of Event
    October 17, 1998
    Product Code
    BYE
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BYE

    Patients

    Seq Age Sex Outcome Treatment
    1