BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    KAPS 90 DEGREE FIBEROPTIC ADAPTOR

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909128852·REVELATION DIAMOND 856-014SC-S - 5 PACK

    SYNCHRON (R) SYSTEMS CREATININE REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code CGX·July 2, 2011

    NEUROMOVE NM900

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ZIMMER PLATES AND SCREWS SYSTEM SCREWS ONLY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH LTD / HUNTINGTON·Product code HQL·November 11, 2010

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 30, 2012

    5.0MM TI LOCKING HEAD SCREW SELF-TAPPING 42MM

    FDA Adverse Event
    Injury ·SYNTHES HAGENDORF·Product code KTT·July 3, 2014