BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1831750-1997-00003

    MDR report key: 77828 · Received March 13, 1997

    Report

    Report Number
    1831750-1997-00003
    Event Type
    Malfunction
    Date Received
    March 13, 1997
    Date of Event
    February 28, 1997
    Product Code
    FPO
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FPO

    Patients

    Seq Age Sex Outcome Treatment
    1