BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    DILATATION CATHETER, BALLOON

    FDA 510(k)
    FDA Unclassified ·Unknown

    Arsenal Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO: ORLUS MINI SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    FLEXI-SEAL SIGNAL FECAL MGMT SYSTEM KIT

    FDA Adverse Event
    Malfunction ·CONVATEC·Product code KNT·May 20, 2014

    CARELINK

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

    MEDISENSE OPTIUM

    FDA Adverse Event
    Malfunction ·Product code NBW·January 7, 2011