BEUDAMED
    FDA Adverse Event Other Summary report: N

    2951413-2001-00007

    MDR report key: 351775 · Received September 13, 2001

    Report

    Report Number
    2951413-2001-00007
    Event Type
    Other
    Date Received
    September 13, 2001
    Date of Event
    August 14, 2001
    Product Code
    MAF
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    41856 MAF

    Patients

    Seq Age Sex Outcome Treatment
    1