BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    SYNTHES SCHUHLI IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    X-FORCE NEPHROSTOMY BALLOON DILATION CATHETER

    FDA 510(k)
    FDA Unclassified ·Unknown

    LIQUID CHROMATOGRAPH MODEL 850

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    TARGET ADAPTER T2 SCN

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 21, 2012

    VERSACARE FRAME

    FDA Adverse Event
    Injury ·HILL-ROM, INC.·Product code FNL·February 19, 2013

    COULTER® HMX HEMATOLOGY ANALYZER WITH AUTOLOADER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·February 8, 2011

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·July 22, 2014