BEUDAMED
    FDA Adverse Event Death Summary report: N

    3024006-1998-00003

    MDR report key: 176943 · Received July 15, 1998

    Report

    Report Number
    3024006-1998-00003
    Event Type
    Death
    Date Received
    July 15, 1998
    Date of Event
    May 6, 1998
    Report Date
    July 14, 1998
    Manufacturer
    UTAH MEDICAL PRODUCTS, INC.
    Product Code
    HDB
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HDB UTAH MEDICAL PRODUCTS, INC. NA 370187

    Patients

    Seq Age Sex Outcome Treatment
    1