BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRUWAVE DISPOSABLE PRESSURE TRANSDUCER

    MDR report key: 1082668 · Received July 21, 2008

    Report

    Report Number
    6000002-2008-07975
    Event Type
    Malfunction
    Date Received
    July 21, 2008
    Date of Event
    June 4, 2008
    Report Date
    June 4, 2008
    Manufacturer
    EDWARDS LIFESCIENCES
    Product Code
    DRS
    PMA / PMN Number
    K832907
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION: DEVICE HAS NOT YET BEEN RETURNED FOR EVALUATION.

    Description of Event or Problem · 1

    CRACK WAS OBSERVED ON THE FEMALE LUER ON THE TRANSDUCER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRUWAVE DISPOSABLE PRESSURE TRANSDUCER DISPOSABLE PRESSURE MONITOR DRS EDWARDS LIFESCIENCES 500488003 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK