BEUDAMED
    FDA Adverse Event Other Summary report: N

    CIRCON ACMI

    MDR report key: 117154 · Received August 1, 1997

    Report

    Report Number
    117154
    Event Type
    Other
    Date Received
    August 1, 1997
    Date of Event
    July 14, 1997
    Report Date
    July 21, 1997
    Manufacturer
    AMERICAN CYSTOSCOPE MAKERS INC.
    Product Code
    FDC
    Report Source
    User Facility report
    Reporter Location
    AR, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    RESECTOSCOPE ACMI IWE PLASTIC THUMB CONTROL BROKE. PURCHASED 2/92.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CIRCON ACMI IGLESIAS RESECTOSCOPE FDC AMERICAN CYSTOSCOPE MAKERS INC. IWE *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other