BEUDAMED
    FDA Adverse Event Injury Summary report: N

    3024006-1998-00005

    MDR report key: 180658 · Received August 5, 1998

    Report

    Report Number
    3024006-1998-00005
    Event Type
    Injury
    Date Received
    August 5, 1998
    Date of Event
    June 29, 1998
    Product Code
    HDB
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1