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

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    Filters Regulation: Us FDA ×

    NeuraGen 3D Nerve Guide Matrix

    FDA 510(k)
    FDA Class 2 ·Neurology

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221046406·Unitek(TM) Molar Band General Purpose Wide Hard...

    TRUEHD (1080P) DIGITAL CAMERA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HYDROCOIL EMBOLIC SYSTEM (HES)

    FDA 510(k)
    FDA Class 2 ·Neurology

    MECATCER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 36 SIZE M 0

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 19, 2017

    ALINITY S HBSAG REAGENT KIT

    FDA Adverse Event
    Injury ·ABBOTT IRELAND·Product code QHM·May 4, 2022

    EASYTRAK 2

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·July 15, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 11, 2013

    REVEAL XT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code DSI·October 10, 2014

    VALIANT CAPTIVIA ENDOVASCULAR STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·August 31, 2017

    VALIANT CAPTIVIA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·September 1, 2017

    VALIANT CAPTIVIA ENDOVASCULAR STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·August 31, 2017

    TALENT THORACIC - XCELERANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·August 31, 2017

    VALIANT CAPTIVIA ENDOVASCULAR STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·August 31, 2017