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

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    SODEM PERFORATOR DRIVE

    FDA 510(k)
    FDA Class 2 ·Neurology

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HET·June 8, 2006

    CLUB FOOT CPM MACHINE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    THERASTIM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    INDIGO 1.0CM LASER FIBER

    FDA Adverse Event
    Death ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GEX·June 22, 2006

    TAXUS EXPRESS2 PACLITAXEL ELUTING STENT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code NIQ·August 7, 2006

    AO/ASIF-QC F/532.001 532.010 532.101 532

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·March 8, 2013

    LEAD MODEL 302

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 11, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014