BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 534911 · Received July 15, 2004

    Report

    Report Number
    1825034-2004-00066
    Event Type
    Death
    Date Received
    July 15, 2004
    Date of Event
    June 23, 2004
    Manufacturer
    BIOMET, INC.
    Product Code
    LOD
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * LOD BIOMET, INC. NA 003586

    Patients

    Seq Age Sex Outcome Treatment
    1 *