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

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    MENSTRUAL TAMPON

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Epic Extremity Cannulated Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EAGLEVISION GELLANSERTS, MODEL REF 0040

    FDA 510(k)
    FDA Unclassified ·Unknown

    VERSYS FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LPH·February 25, 2016

    CARELINK

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 9, 2013

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KDI·July 23, 2014

    REPLACEMENT HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·January 7, 2011