BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STORZ PROTEGE OPHTHALMIC MICROSURGICAL SYSTEM

    MDR report key: 36850 · Received August 30, 1996

    Report

    Report Number
    1920664-1996-00602
    Event Type
    Malfunction
    Date Received
    August 30, 1996
    Date of Event
    August 1, 1996
    Report Date
    August 2, 1996
    Manufacturer
    STORZ INSTRUMENT CO.
    Product Code
    HQE
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    DURING A CATARACT EXTRACTION PROCEDURE, THIS OPHTHALMIC MICROSURGICAL SYSTEM EXHIBITED POWER SURGES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STORZ PROTEGE OPHTHALMIC MICROSURGICAL SYSTEM OPHTHALMIC MICROSURGICAL SYSTEM HQE STORZ INSTRUMENT CO. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO