BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1920664-2000-00002

    MDR report key: 267840 · Received March 7, 2000

    Report

    Report Number
    1920664-2000-00002
    Event Type
    Injury
    Date Received
    March 7, 2000
    Date of Event
    January 12, 2000
    Product Code
    HQC
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1