BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1920664-2002-00052

    MDR report key: 386198 · Received April 3, 2002

    Report

    Report Number
    1920664-2002-00052
    Event Type
    Injury
    Date Received
    April 3, 2002
    Date of Event
    February 18, 2002
    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