BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 967892 · Received May 25, 2006

    Report

    Report Number
    1017072-2006-00002
    Event Type
    Other
    Date Received
    May 25, 2006
    Manufacturer
    COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
    Product Code
    JOW
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THIS COMPLAINT IS CURRENTLY UNDER INVESTIGATION; UPON RECEIPT OF THE RESULTS, THEY WILL BE FORWARDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * JOW COVIDIEN LP, FORMERLY REGISTERED AS KENDALL * *

    Patients

    Seq Age Sex Outcome Treatment
    1