BEUDAMED
    FDA Adverse Event Other Summary report: N

    9610614-1999-00002

    MDR report key: 218304 · Received April 9, 1999

    Report

    Report Number
    9610614-1999-00002
    Event Type
    Other
    Date Received
    April 9, 1999
    Date of Event
    March 18, 1999
    Product Code
    MNJ
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1