BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    DIAGNOST 76 FAMILY*R/F SYSTEMS - RELEASE 4.4

    FDA 510(k)
    FDA Class 2 ·Radiology

    CERAMIC FEMORAL HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEMOCHRON/FACTOR VI FIBRINOGEN ASSAY AND CONT PLAS

    FDA 510(k)
    FDA Class 2 ·Hematology

    SUMMIT CEMENTED STEM SZ3 STD

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD.·Product code JDI·January 22, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010

    OT VERIO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 10, 2014