BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    NERVE STIMULATOR, MOLEL NO. FB-800

    FDA 510(k)
    FDA Class 2 ·Neurology

    Captus Vascular Retrieval System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SENTINEL LITHIUM ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·November 13, 2007

    TRIMA ACCEL

    FDA Adverse Event
    TERUMO BCT·Product code GKT·October 3, 2012

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·December 18, 2013