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

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    MODIFICATION TO FIDIS VASCULITIS, MODEL MX007

    FDA 510(k)
    FDA Class 2 ·Immunology

    THE MAESTRO SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    URINE BENZODIAZEPINES (BENZ) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF 92A

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    INCEPTA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 22, 2013

    EXPRESS VASCULAR LD PREMOUNTED STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·April 27, 2011

    ANALYTICAL P MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·July 7, 2008