BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    TICK-ATTACK(TM) KIT

    FDA 510(k)
    FDA Not Classified ·Unknown

    ihcDirect® Pan-CK 4Abs

    FDA UDI
    NOVODIAX, INC.·00850000596214·Clones AE1/AE3, C94, R226

    BIPOLAR FORCEPS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CORD STICK MULTIPLE DRAW SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 28, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·December 17, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 14, 2014

    LAUNCHER UNK GUIDE CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC, INC·Product code DQY·January 19, 2022