BEUDAMED
    FDA Adverse Event Other Summary report: N

    ABBOTT

    MDR report key: 137042 · Received July 5, 1997

    Report

    Report Number
    MW1012617
    Event Type
    Other
    Date Received
    July 5, 1997
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    FPA
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    UNK

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT EXT. SET FPA ABBOTT LABORATORIES * *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other