BEUDAMED
    FDA Adverse Event Other Summary report: N

    1043572-2001-00003

    MDR report key: 336707 · Received June 4, 2001

    Report

    Report Number
    1043572-2001-00003
    Event Type
    Other
    Date Received
    June 4, 2001
    Date of Event
    November 29, 2000
    Report Date
    December 14, 2000
    Manufacturer
    STERIS CORP
    Product Code
    FQO
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    25645 FQO STERIS CORP NA

    Patients

    Seq Age Sex Outcome Treatment
    1