BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ULTRAFINE ERBIUM SYSTEM

    MDR report key: 220189 · Received April 23, 1999

    Report

    Report Number
    2914019-1999-00001
    Event Type
    Injury
    Date Received
    April 23, 1999
    Date of Event
    March 22, 1999
    Report Date
    April 7, 1999
    Manufacturer
    COHERENT MEDICAL GROUP
    Product Code
    GEX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING FACIAL RESURFACING TREATMENT WITH ULTRAFINE LASER, THE PT EXPERIENCED CARDIAC ARREST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ULTRAFINE ERBIUM SYSTEM SURGICAL LASERS GEX COHERENT MEDICAL GROUP NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Hospitalization| L