BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    KERR PORCELAIN REPAIR PRIMER

    FDA 510(k)
    FDA Class 2 ·Dental

    Endo Model Knee Fusion Nail FK

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575346721·Femoral Component

    Nitinol Compression Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRUITT-INAHARA OUTLYING CAROTID SHUNT, MODELS, 2012-49, 2013-49, 2014-49,2015-49,2016-49, 2017-49

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    Zimmer, Inc.·00889024195233·

    INRATIO PT/INR TEST STRIP

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·March 14, 2014

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·November 21, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2015