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

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    Filters Regulation: Us FDA ×

    RootMend MRR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SOFT PLUG Extended Duration 180 Tapered Canalicular Plug

    FDA 510(k)
    FDA Unclassified ·Unknown

    Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·November 11, 2014

    ANESTHESIA MACHINE

    FDA Adverse Event
    Injury ·DATEX-OHMEDA·Product code BSZ·September 7, 2011

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 24, 2013

    X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300 103-0601-350V10 103-0602-350V06 103-0601-300V01 103-0602-300 103-0602-350V09 103-0601-300V02 103-0602-300V01 103-0602-350V10 103-0601-300V03 103-0602-300V02 103-0601-300V06 103-0602-300v06 103-0601-300V10 103-0602-300V09 103-0601-300V11 103-0602-300V10 103-0601-350 103-0602-350 103-0601-350V01 103-0602-350V01 103-0601-350V06 103-0602-350V02

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·November 16, 2016