BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    EMIT AED PHENYTOIN ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ihcDirect® Cytokeratin 19 Ab

    FDA UDI
    NOVODIAX, INC.·00850000596450·Clone R1002

    ihcDirect® Cytokeratin 19 Ab

    FDA UDI
    NOVODIAX, INC.·00850000596443·Clone R1002

    ihcDirect® Cytokeratin 19 Ab Conjugate 15mL

    FDA UDI
    NOVODIAX, INC.·00850030934208·Clone R1002

    ihcDirect® Cytokeratin 19 Ab Conjugate 5mL

    FDA UDI
    NOVODIAX, INC.·00850030934192·Clone R1002

    BM3/BM3 PLUS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    V SERIES MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·March 7, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 14, 2012

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 3, 2010