BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1220290-1999-00002

    MDR report key: 242885 · Received September 29, 1999

    Report

    Report Number
    1220290-1999-00002
    Event Type
    Injury
    Date Received
    September 29, 1999
    Date of Event
    September 3, 1999
    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