BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    THREE-PC. SYRINGES 2-30 ML, W. MOUNT. N

    MDR report key: 3896987 · Received June 3, 2014

    Report

    Report Number
    9610825-2014-00218
    Event Type
    Malfunction
    Date Received
    June 3, 2014
    Manufacturer
    B. BRAUN MELSUNGEN AG
    Product Code
    FMF
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE INVESTIGATION IS ON GOING AT THIS TIME. A FOLLOW UP REPORT WILL BE PROVIDED AFTER THE INSPECTION RESULTS BECOME AVAILABLE.

    Description of Event or Problem · 1

    (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    325352 THREE-PC. SYRINGES 2-30 ML, W. MOUNT. N SYRINGES FMF B. BRAUN MELSUNGEN AG

    Patients

    Seq Age Sex Outcome Treatment
    1