BEUDAMED
    FDA Adverse Event Other Summary report: N

    2951413-2001-00008

    MDR report key: 361426 · Received November 9, 2001

    Report

    Report Number
    2951413-2001-00008
    Event Type
    Other
    Date Received
    November 9, 2001
    Date of Event
    October 12, 2001
    Product Code
    MAF
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    50544 MAF

    Patients

    Seq Age Sex Outcome Treatment
    1