BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 394413 · Received January 30, 2002

    Report

    Report Number
    2925153-2001-00019
    Event Type
    Other
    Date Received
    January 30, 2002
    Date of Event
    December 17, 2001
    Manufacturer
    HDC CORP.
    Product Code
    DQO
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * DQO HDC CORP. * *

    Patients

    Seq Age Sex Outcome Treatment
    1