BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    MiiS Horus Bronchoscope; MiiS Horus Endoscope Display System -Tablet; MiiS Horus Endoscope Display System -Video Box

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

    Arthrex FiberTak Suture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Hand-held IPL device(JOVS Graphene Hair Removal Device)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·February 28, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 7, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·August 30, 2011

    PROLENE HERNIA SYSTEM MESH

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·July 18, 2013