BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 340861 · Received July 3, 2001

    Report

    Report Number
    1047429-2001-00001
    Event Type
    Other
    Date Received
    July 3, 2001
    Date of Event
    May 10, 2001
    Manufacturer
    AVID MEDICAL, INC.
    Product Code
    LRO
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    30074 * CUSTOM PROCEDURE TRAY LRO AVID MEDICAL, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 Other