BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FAVOLORO-MORSE STERNAL SPREADER

    MDR report key: 534695 · Received January 7, 2004

    Report

    Report Number
    2515651-2003-00006
    Event Type
    Malfunction
    Date Received
    January 7, 2004
    Date of Event
    October 31, 2003
    Manufacturer
    PILLING SURGICAL
    Product Code
    FFO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FAVOLORO-MORSE STERNAL SPREADER SELF-RETAINING RETRACTOR FFO PILLING SURGICAL 34-1164 SS-3

    Patients

    Seq Age Sex Outcome Treatment
    1 *