BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    BRIGHTSTAR

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

    AXSOS

    FDA UDI
    Stryker GmbH·07613154728992·X-Ray Template - Prox. Lat. Tibia Plate TS

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981081·anteriors; shade A3.5; mould CL2

    Infrared Ear Thermometer

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ZOLL E SERIES WITH BLUETOOTH DIAL UP NETWORKING

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    DEXTRUS 4135

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·February 19, 2013

    MAXI MOVE (AHE)

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·January 27, 2011

    IMPULSE GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQO·August 5, 2014