BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2951413-2001-00010

    MDR report key: 365001 · Received December 5, 2001

    Report

    Report Number
    2951413-2001-00010
    Event Type
    Injury
    Date Received
    December 5, 2001
    Date of Event
    November 5, 2001
    Product Code
    ---
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    54615 ---

    Patients

    Seq Age Sex Outcome Treatment
    1