BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    3004659744-2008-00004_

    MDR report key: 1031580 · Received March 19, 2008

    Report

    Report Number
    3004659744-2008-00004_
    Event Type
    Malfunction
    Date Received
    March 19, 2008
    Product Code
    JAK
    PMA / PMN Number
    K042438
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THE RETURN OF THE DEVICE IS PENDING.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1