BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VIDAS® CMV IGM

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code LKQ·July 6, 2018

    VIDAS® CMV IGM

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code LKQ·September 8, 2017

    VIDAS® CMV IGM

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, S.A.·Product code LKQ·September 7, 2017

    VIDAS® CMV IGM

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, S.A.·Product code LKQ·September 14, 2017

    VIDAS® CMV IGM

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, S.A.·Product code LKQ·September 7, 2017

    VIDAS® CMV IGM

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, S.A.·Product code LKQ·September 14, 2017

    VIDAS® CMV IGM

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code LKQ·September 6, 2017

    VIDAS® CMV IGM

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code LKQ·September 6, 2017

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·May 9, 2014

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·October 24, 2012

    SIGMA 300 D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·August 17, 2010