BEUDAMED
    FDA Adverse Event Injury Summary report: N

    8010047-1997-00015

    MDR report key: 97445 · Received June 11, 1997

    Report

    Report Number
    8010047-1997-00015
    Event Type
    Injury
    Date Received
    June 11, 1997
    Date of Event
    May 5, 1997
    Product Code
    HEZ
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1