BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD DTX PLUS

    MDR report key: 1000718 · Received February 19, 2008

    Report

    Report Number
    8020616-2008-00009
    Event Type
    Malfunction
    Date Received
    February 19, 2008
    Report Date
    November 26, 2007
    Manufacturer
    BECTON DICKINSON CRITICAL CARE SYSTEMS, PTE., LTD.
    Product Code
    DRS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    UNKNOWN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD DTX PLUS DISPOSABLE PRESSURE TRANSDUCER WITH PRESSURE MONITORING SET DRS BECTON DICKINSON CRITICAL CARE SYSTEMS, PTE., LTD. NA 706278

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK