BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    2D Quantitative Analysis

    FDA 510(k)
    FDA Class 2 ·Radiology

    KANEKA PHARMA AMERICA XPRESS-WAY RX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIMENSION VISTA DBIL FLEX REAGENT CARTRIDGE, MODEL K2125

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929066379·Corpectomy, 16Dx18Wx39H 6°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929066003·Corpectomy, 16Dx18Wx39H 0°

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·June 11, 2013

    TRIFECTA VALVE

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL BRASIL LTDA·Product code LWR·July 8, 2011

    ATTAIN ABILITY PLUS

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·October 10, 2014

    THROMBUSTER II

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code MMY·March 17, 2014

    THROMBUSTER II

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code DXE·October 23, 2012

    THROMBUSTER II

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code DXE·December 21, 2012

    THROMBUSTER II

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code DXE·January 16, 2019