BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2951413-2002-00002

    MDR report key: 387684 · Received April 1, 2002

    Report

    Report Number
    2951413-2002-00002
    Event Type
    Malfunction
    Date Received
    April 1, 2002
    Date of Event
    March 13, 2002
    Product Code
    MAF
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1