BEUDAMED
    FDA Adverse Event Other Summary report: N

    2431021-1998-00011

    MDR report key: 196896 · Received November 12, 1998

    Report

    Report Number
    2431021-1998-00011
    Event Type
    Other
    Date Received
    November 12, 1998
    Date of Event
    September 23, 1998
    Report Date
    November 11, 1998
    Manufacturer
    MILTEX INSTRUMENT CO, INC.
    Product Code
    EAX
    Adverse Event
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EAX MILTEX INSTRUMENT CO, INC. UNK

    Patients

    Seq Age Sex Outcome Treatment
    1