BEUDAMED
    4 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    MAXIMO II VR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·February 9, 2013

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·July 23, 2014

    GENERATOR MODEL UNKNOWN

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·January 5, 2011