BEUDAMED
    FDA Adverse Event Death Summary report: N

    USA SERIES M2 TELESCOPE

    MDR report key: 300404 · Received October 11, 2000

    Report

    Report Number
    1218764-2000-00013
    Event Type
    Death
    Date Received
    October 11, 2000
    Date of Event
    September 6, 2000
    Report Date
    October 11, 2000
    Manufacturer
    CIRCON ACMI
    Product Code
    FBP
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 USA SERIES M2 TELESCOPE TELESCOPE FBP CIRCON ACMI M2- NA

    Patients

    Seq Age Sex Outcome Treatment
    1 SERIES CYSTOURETHROSCOPE SHEATH WITH OBTURATOR.| SHEATH WITH OBTURATOR, G121, USA SERIES/CLASSIC| G117, USA SERIES/CLASSIC SERIES CYSTOURETHROSCOPE