BEUDAMED
    FDA Adverse Event Other Summary report: N

    1043572-2001-00006

    MDR report key: 355809 · Received October 10, 2001

    Report

    Report Number
    1043572-2001-00006
    Event Type
    Other
    Date Received
    October 10, 2001
    Date of Event
    August 21, 2001
    Manufacturer
    STERIS CORP
    Product Code
    FQO
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    46040 FQO STERIS CORP NA

    Patients

    Seq Age Sex Outcome Treatment
    1