BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRUWAVE DISPOSABLE PRESSURE TRANSDUCER

    MDR report key: 1082666 · Received July 21, 2008

    Report

    Report Number
    6000002-2008-07978
    Event Type
    Malfunction
    Date Received
    July 21, 2008
    Date of Event
    May 3, 2008
    Report Date
    June 12, 2008
    Manufacturer
    EDWARDS LIFESCIENCES
    Product Code
    DRS
    PMA / PMN Number
    K925638
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KN
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION: DEVICE HAS NOT BEEN RETURNED AT THIS TIME FOR EVALUATION.

    Description of Event or Problem · 1

    IT WAS REPORTED THE CONNECTOR PARTS BETWEEN TRANSDUCER AND IV LINE ARE BROKEN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRUWAVE DISPOSABLE PRESSURE TRANSDUCER DISPOSABLE PRESSURE MONITOR DRS EDWARDS LIFESCIENCES PX260 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK