BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    USA MRO-7 INTEGRAL OPERATING URETEROSCOPE

    MDR report key: 159314 · Received March 24, 1998

    Report

    Report Number
    1218764-1998-00006
    Event Type
    Malfunction
    Date Received
    March 24, 1998
    Report Date
    February 27, 1998
    Manufacturer
    CIRCON ACMI
    Product Code
    FGB
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INSTRUMENT REPORTEDLY BENT UNDER NORMAL OPERATING CONDITIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 USA MRO-7 INTEGRAL OPERATING URETEROSCOPE URETEROSCOPE FGB CIRCON ACMI MRO-733 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO