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

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    Filters Regulation: Us FDA ×

    Headless Compression Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814275·GENUMEDI PT SILVER R IV

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A14362480·14mm H x 36mm W x 24mm L x 8 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A143624120·14mm H x 36mm W x 24mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A143624150·14mm H x 36mm W x 24mm L x 15 degrees ALIF

    WONDFO BUPRENORPHINE URINE TEST WONDFO OXYCODONE URINE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    OTOSTAT DPOAE + MEPA MEASUREMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Added Screen Displays For FDA Cleared HeartSee Cardiac P.E.T Processing Software K143664

    FDA 510(k)
    FDA Class 2 ·Radiology

    2520274-2013-02917

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·June 3, 2013

    LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·June 3, 2011

    SMARTSETMV MV ENDURANCE 40 G

    FDA Adverse Event
    Injury ·DEPUY CMW·Product code LOD·August 28, 2008

    BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·March 15, 2018