BEUDAMED
    FDA Adverse Event Summary report: N

    2020364-1997-00023

    MDR report key: 134197 · Received November 19, 1997

    Report

    Report Number
    2020364-1997-00023
    Date Received
    November 19, 1997
    Date of Event
    October 20, 1997
    Product Code
    BZW
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1