BEUDAMED
    FDA Adverse Event Death Summary report: N

    1119193-1998-00002

    MDR report key: 174426 · Received June 26, 1998

    Report

    Report Number
    1119193-1998-00002
    Event Type
    Death
    Date Received
    June 26, 1998
    Date of Event
    May 2, 1998
    Product Code
    CBH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1