BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MK SYRINGE 3-P, LL 10CC

    MDR report key: 3854213 · Received May 29, 2014

    Report

    Report Number
    9610825-2014-00205
    Event Type
    Malfunction
    Date Received
    May 29, 2014
    Manufacturer
    B. BRAUN MELSUNGEN AG
    Product Code
    FMF
    PMA / PMN Number
    K071459
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE INVESTIGATION INTO THE REPORTED EVENT IS ON GOING AT THIS TIME. A FOLLOW UP REPORT WILL BE PROVIDED WHEN THE INVESTIGATION RESULTS BECOME AVAILABLE.

    Description of Event or Problem · 1

    (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    317337 MK SYRINGE 3-P, LL 10CC SYRINGES FMF B. BRAUN MELSUNGEN AG

    Patients

    Seq Age Sex Outcome Treatment
    1