BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    AORTIC ARCH CANNULAS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODEL {M-102 I-CHANNEL ELECTRO CARDIOGRAPH UNIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Stable-L Lumbar Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·July 27, 2015

    TAXUS® LIBERTÉ® LONG

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·February 5, 2013

    FORTIFY ASSURA DR, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 18, 2014