BEUDAMED
    4 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    URIC ACID REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code KNK·April 15, 2011

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·March 6, 2013

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIM·February 15, 2011

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWP·August 8, 2014