BEUDAMED
    7 results · 29ms · Sources: EU EUDAMED, US FDA

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    SURGITRON

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

    ACCESS CARDIOSYSTEMS MANUAL DEFIBRILLATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Exofin Fusion Skin Closure System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VENTAK PRIZM 2

    FDA Adverse Event
    Injury ·GUIDANT CLONMEL IRELAND·Product code LWS·January 11, 2013

    UMBILI-CATH

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC·Product code FOS·November 17, 2010

    MBT TIBIAL IMPACTOR

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·July 3, 2014

    VITEK® 2 AST-GN80 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·October 18, 2017