BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2183161-1996-00001

    MDR report key: 41874 · Received September 13, 1996

    Report

    Report Number
    2183161-1996-00001
    Event Type
    Malfunction
    Date Received
    September 13, 1996
    Date of Event
    August 5, 1996
    Manufacturer
    GRASEBY MEDICAL, INC.
    Product Code
    FRN
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FRN GRASEBY MEDICAL, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 *