BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2951413-2001-00004

    MDR report key: 353355 · Received September 7, 2001

    Report

    Report Number
    2951413-2001-00004
    Event Type
    Injury
    Date Received
    September 7, 2001
    Date of Event
    August 10, 2001
    Product Code
    MAF
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    40725 MAF

    Patients

    Seq Age Sex Outcome Treatment
    1