BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NONE

    MDR report key: 2212434 · Received March 1, 2006

    Report

    Report Number
    1713747-2006-00063
    Event Type
    Injury
    Date Received
    March 1, 2006
    Report Date
    February 27, 2006
    Manufacturer
    OGDEN MANUFACTURING
    Product Code
    KDI
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SERIOUS INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NONE KDI OGDEN MANUFACTURING NA

    Patients

    Seq Age Sex Outcome Treatment
    1