BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MAQUET CARDIOPULMONARY AG

    MDR report key: 3676474 · Received February 11, 2014

    Report

    Report Number
    8010762-2014-00046
    Event Type
    Injury
    Date Received
    February 11, 2014
    Manufacturer
    MAQUET CARDIOPULMONARY AG
    Product Code
    DTQ
    PMA / PMN Number
    K943803
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). MAQUET (B)(4) PROVIDES PRODUCT FAILURE INVESTIGATION, ANALYSIS AND RESOLUTION FOR THE DEVICE DESCRIBED IN THIS REPORT. A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED IF ADDITIONAL BECOMES AVAILABLE. (B)(4). THIS EVENT IS RELATED TO MEDWATCH REPORT #8010762-2014-00045 AND 3008355164-2014-00014.

    Description of Event or Problem · 1

    PLEASE REFER IMPORTER REPORT #: (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    88966 MAQUET CARDIOPULMONARY AG HL 20 CONSOLE BASE DTQ MAQUET CARDIOPULMONARY AG

    Patients

    Seq Age Sex Outcome Treatment
    1