BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STORZ THORNTON FIXATION RING W/HANDLE

    MDR report key: 66381 · Received January 31, 1997

    Report

    Report Number
    1932180-1997-00018
    Event Type
    Malfunction
    Date Received
    January 31, 1997
    Date of Event
    January 2, 1997
    Report Date
    January 2, 1997
    Manufacturer
    STORZ INSTRUMENT CO.
    Product Code
    HNH
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INSTRUMENT BROKE DURING AN OPHTHALMIC PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STORZ THORNTON FIXATION RING W/HANDLE OPHTHALMIC RING HNH STORZ INSTRUMENT CO. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO