BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FZP

    MDR report key: 966064 · Received November 15, 2006

    Report

    Report Number
    1527736-2006-05938
    Event Type
    Malfunction
    Date Received
    November 15, 2006
    Report Date
    October 23, 2006
    Product Code
    FZP
    PMA / PMN Number
    K050344
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    INFORMATION ANTICIPATED, BUT UNAVAILABLE AT THIS TIME.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1