BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1920664-2001-00043

    MDR report key: 378520 · Received December 12, 2001

    Report

    Report Number
    1920664-2001-00043
    Event Type
    Injury
    Date Received
    December 12, 2001
    Date of Event
    October 26, 2001
    Product Code
    MOE
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    56661 MOE

    Patients

    Seq Age Sex Outcome Treatment
    1