BEUDAMED
    FDA Adverse Event Death Summary report: N

    MAQUET O.R. TABLE SYSTEM MAGNUS

    MDR report key: 3721981 · Received March 25, 2014

    Report

    Report Number
    8010652-2014-00007
    Event Type
    Death
    Date Received
    March 25, 2014
    Manufacturer
    MAQUET GMBH
    Product Code
    FQO
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    MAQUET IS WORKING WITH THE HOSPITAL TO REMOVE THE MAGNUS TABLE. THE CUSTOMER HAS ELECTED TO INSTALL A THIRD PARTY DEVICE IN ITS PLACE. TABLE IS PRESENTLY IN USE BY HOSPITAL UNTIL ITS REPLACEMENT IS INSTALLED. (B)(4). MAQUET MEDICAL SYSTEMS USA SUBMITS THIS REPORT ON BEHALF OF THE DEVICE MFG FACILITY. MAQUET (B)(4) PROVIDES PRODUCT FAILURE INVESTIGATION, ANALYSIS AND RESOLUTION FOR THE DEVICE DESCRIBED IN THIS REPORT.

    Description of Event or Problem · 1

    (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    173767 MAQUET O.R. TABLE SYSTEM MAGNUS FQO & KXJ-TABLE,AC POWERED & RADIOLOGIC FQO MAQUET GMBH

    Patients

    Seq Age Sex Outcome Treatment
    1