BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GEI

    MDR report key: 967155 · Received June 30, 2006

    Report

    Report Number
    1527736-2006-03014
    Event Type
    Malfunction
    Date Received
    June 30, 2006
    Manufacturer
    ETHICON ENDO SURGERY, INC. (CINCINNATI)
    Product Code
    GEI
    PMA / PMN Number
    K002981
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    INFO ANTICIPATED, BUT UNAVAILABLE AT THIS TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GEI GEI ETHICON ENDO SURGERY, INC. (CINCINNATI) NA

    Patients

    Seq Age Sex Outcome Treatment
    1 GENERATOR| HANDPIECE