BEUDAMED
    FDA Adverse Event Other Summary report: N

    MONARCH CORE INSTRUMENT CASE

    MDR report key: 670651 · Received January 31, 2006

    Report

    Report Number
    1526439-2006-00027
    Event Type
    Other
    Date Received
    January 31, 2006
    Date of Event
    December 16, 2005
    Manufacturer
    DEPUY SPINE INC.
    Product Code
    LRP
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MONARCH CORE INSTRUMENT CASE SURGICAL INSTRUMENT CASE/TRAY LRP DEPUY SPINE INC. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1