BEUDAMED
    4 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·November 7, 2013

    COULTER® AC*T DIFF ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·March 5, 2013

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·February 8, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014