BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1920664-2006-00049

    MDR report key: 969090 · Received May 22, 2006

    Report

    Report Number
    1920664-2006-00049
    Event Type
    Injury
    Date Received
    May 22, 2006
    Product Code
    HQC
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1