BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2925153-2000-00002

    MDR report key: 270576 · Received March 14, 2000

    Report

    Report Number
    2925153-2000-00002
    Event Type
    Injury
    Date Received
    March 14, 2000
    Date of Event
    January 3, 2000
    Product Code
    DQO
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1