BEUDAMED
    FDA Adverse Event Other Summary report: N

    VERSAPULSE AESTHETIC C

    MDR report key: 121403 · Received September 19, 1997

    Report

    Report Number
    2914019-1997-00025
    Event Type
    Other
    Date Received
    September 19, 1997
    Date of Event
    July 21, 1997
    Report Date
    August 20, 1997
    Manufacturer
    COHERENT MEDICAL LASER GROUP
    Product Code
    GEX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    VASCULAR BLUSHING RESULTED AFTER DOCTOR DID A LEG VEIN TREATMENT (LOWER LEG).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSAPULSE AESTHETIC C SURGICAL LASER GEX COHERENT MEDICAL LASER GROUP 0626-472-01 *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other