BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2020394-1997-00002

    MDR report key: 88912 · Received May 1, 1997

    Report

    Report Number
    2020394-1997-00002
    Event Type
    Injury
    Date Received
    May 1, 1997
    Date of Event
    March 25, 1997
    Product Code
    MCI
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *