BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SINGLE DISP TRANSPAC IV TRANSDUCER

    MDR report key: 506921 · Received December 23, 2003

    Report

    Report Number
    1713468-2003-00073
    Event Type
    Malfunction
    Date Received
    December 23, 2003
    Date of Event
    November 25, 2003
    Report Date
    November 27, 2003
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    BYR
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SINGLE DISP TRANSPAC IV TRANSDUCER PRESSURE MONITORING KIT BYR ABBOTT LABORATORIES NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 34 YR Other