BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    LnK Anterior Cervical Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MINI TREK RX CORONARY DILATATION CATHETER (INCLUDING 1.20 MM SIZE), MINI TREK OTW CORONARY DILATATION CATHETER (INCLUDIN

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IDENTIUM HEAVY, IDENTIUM MEDIUM, IDENTIUM SCAN HEAVY, IDENTIUM SCAN MEDIUM, IDENTIUM SCAN LIGHT

    FDA 510(k)
    FDA Class 2 ·Dental

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 16, 2015

    PEDICSCR PANGEAPOLYAX Ø6 PREASSMBL L40 T

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code NKB·June 3, 2013

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code DTB·January 13, 2014

    PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 28, 2011

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 16, 2013