BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SAFE-T-CENTESIS

    MDR report key: 3201016 · Received May 23, 2013

    Report

    Report Number
    3201016
    Event Type
    Malfunction
    Date Received
    May 23, 2013
    Date of Event
    May 16, 2013
    Report Date
    May 22, 2013
    Manufacturer
    CAREFUSION
    Product Code
    GCB
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    229524 SAFE-T-CENTESIS CATHETER GCB CAREFUSION * 0000550170

    Patients

    Seq Age Sex Outcome Treatment
    1 *