BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CAREVO

    MDR report key: 3952407 · Received June 18, 2014

    Report

    Report Number
    3007420694-2014-00073
    Event Type
    Injury
    Date Received
    June 18, 2014
    Manufacturer
    ARJOHUNTLEIGH POLSKA SP. Z O.O.
    Product Code
    FNG
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). ADDITIONAL INFORMATION WILL BE PROVIDED UPON CONCLUSION OF THE MANUFACTURER'S INVESTIGATION.

    Description of Event or Problem · 1

    REFERENCE IMPORTER # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    358031 CAREVO FNG ARJOHUNTLEIGH POLSKA SP. Z O.O.

    Patients

    Seq Age Sex Outcome Treatment
    1