BEUDAMED
    FDA Adverse Event Other Summary report: N

    NONE

    MDR report key: 2923381 · Received October 6, 2006

    Report

    Report Number
    9611112-2006-00003
    Event Type
    Other
    Date Received
    October 6, 2006
    Product Code
    KAP
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE MANUFACTURER HAS BEEN NOTIFIED OF THE REPORTED COMPLAINT.

    Description of Event or Problem · 1

    .

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NONE KAP

    Patients

    Seq Age Sex Outcome Treatment
    1