BEUDAMED
    5 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2014

    ACCU-CHEK D-TRONPLUS

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN INFUSION SYSTEMS INC.·Product code LZG·October 17, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 11, 2010

    SMR CEMENTLESS FINNED STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code HSD·March 7, 2019

    FEM. MODULAR HEAD - L Ø36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code LZO·February 6, 2019