BEUDAMED
    86 results · 19ms · Sources: EU EUDAMED, US FDA

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    PAX-UNI3D, PHT-7500

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517574374·CoRoent Ant TLIF Ti, 12x11x40mm 0°

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515234406·Iris Forcep, bipolar, str 0.5mm tip

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702256727·ELVAREX 2/THIGH HIGH/CLOSED TOE, E-VERSION, KNE...

    PHACO CHOPPER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896013117·PHACO CHOPPER ANGLED EDGE TITANIUM

    SafeGuide®

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·00816734021194·Esophageal Dilatation System

    PHACO CHOPPER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896013049·PHACO CHOPPER ANGLED EDGE STAINLESS STEEL

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515016873·Olsen-Hegar N.H., del, serr, 4 3/4"

    Malibu™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981029869·PRECONTOURED TI ROD, 5.5 X 400mm

    LOCKING COMPRESSION PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTETRAK LOGIC CR TIBIAL INSERT, OPTETRAK LOGIC CR FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VuMesh™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981036591·14mm Sq Non-angled End Cap

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·January 3, 2017

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·February 2, 2016

    EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·September 27, 2016

    FGE CATHETER, BILIARY, DIAGNOSTIC - BILIARY STENT - METAL

    FDA Adverse Event
    Injury ·COOK INC·Product code FGE·January 29, 2020

    IDENTITY ADX DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·May 5, 2011

    Salzkonzentrat K2-1400 l

    Basic UDI-DI
    EU MDD · Eu Md Class 2b ·Biochem Bernburg GmbH·1 device