BEUDAMED
    FDA Adverse Event Injury Summary report: N

    6000089-2006-02481

    MDR report key: 789012 · Received November 21, 2006

    Report

    Report Number
    6000089-2006-02481
    Event Type
    Injury
    Date Received
    November 21, 2006
    Product Code
    LIT
    PMA / PMN Number
    K011889
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS NOT BEEN RECEIVED FOR ANALYSIS AS OF THE DATE OF THIS REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIT

    Patients

    Seq Age Sex Outcome Treatment
    1