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

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    MITAKA UNIARM

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

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450213551·

    MAMMOGRAPH

    FDA 510(k)
    FDA Class 2 ·Radiology

    CITRASATE DIALYSATE ACID CONCENTRATE LIQUID, MODELS CS-1XXX-XX, CS-XXX-XX, CS-3XXX-XX

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

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 2, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 15, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·April 26, 2011

    Merit Medical systems, Inc, Convenience Kit REF/CAT no.: K09-07692 REVISION A , CUSTOM KIT

    FDA Recall
    Terminated ·Merit Medical Systems, Inc.·Product code MDM·September 29, 2009

    5.0MM FLEXIBLE SHAFT

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code HTO·February 16, 2017

    5.0MM FLEXIBLE SHAFT

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTO·January 3, 2020

    5.0MM FLEXIBLE SHAFT

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code HTO·February 20, 2017