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

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    Filters FDA Adverse Event ×

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 30, 2014

    ATLANTIS SR PRO CORONARY IMAGING CATHETER, MODEL 38942

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT·Product code DQO·October 22, 2010

    PROPLEGE CORONARY SINUS CATHETER

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DWF·December 19, 2012