BEUDAMED
    4 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LDR SPINE ROI-C INTERBODY FUSION DEVICE

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code MAX·May 30, 2014

    URETERAL CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code GBM·January 4, 2013

    UNICEL® DXC 600I SYNCHRON ® CHEMISTRY ANALYZER

    FDA Adverse Event
    BECKMAN COULTER INC.·Product code JJE·November 11, 2010

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 10, 2019