BEUDAMED
    4 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT MANUFACTURING INC·Product code JJE·April 4, 2019

    SYMBIQ SINGLE CHANNE

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 4, 2014

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 23, 2012

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·August 16, 2010