BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2242551-1996-00012

    MDR report key: 48998 · Received November 7, 1996

    Report

    Report Number
    2242551-1996-00012
    Event Type
    Injury
    Date Received
    November 7, 1996
    Date of Event
    October 31, 1996
    Product Code
    CCW
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1