BEUDAMED
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    KETAC-CONDITIONER

    FDA 510(k)
    FDA Class 2 ·Dental

    SATURN 9000-550

    FDA 510(k)
    FDA Class 2 ·Radiology

    Affinity Pixie Oxygenator with Balance Biosurface, Affinity Pixie Oxygenator with Cardiotomy/Venous Reservoir and Balance Biosurface, Affinity Pixie Oxygenator with Cortiva BioActive Surface, Affinity Fusion Oxygenator with Cardiotomy/Venous Reservoir and Cortiva BioActive Surface

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ONYX AVM

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code MFE·February 18, 2011

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·March 14, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·March 14, 2014

    NX3

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EMA·March 14, 2014

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 13, 2014

    VITROS CHEMISTRY PRODUCTS PHYT SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code DIP·October 18, 2010

    PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 13, 2012