BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1210587 · Received May 12, 2008

    Report

    Report Number
    1527736-2008-02928
    Event Type
    Malfunction
    Date Received
    May 12, 2008
    Manufacturer
    ETHICON ENDO-SURGERY, INC.
    Product Code
    LFL
    PMA / PMN Number
    k042777
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Additional Manufacturer Narrative · 1

    INFO ANTICIPATED, BUT UNAVAILABLE AT THIS TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * LFL ETHICON ENDO-SURGERY, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 HANDPIECE| GENERATOR