BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2925153-2000-00018

    MDR report key: 320441 · Received January 29, 2001

    Report

    Report Number
    2925153-2000-00018
    Event Type
    Injury
    Date Received
    January 29, 2001
    Date of Event
    November 25, 2000
    Product Code
    ---
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    3967 ---

    Patients

    Seq Age Sex Outcome Treatment
    1