BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MITROFLOW AORTIC PERICARDIAL HEART VALVE

    FDA Adverse Event
    Injury ·SORIN GROUP CANADA INC.·Product code DYE·October 9, 2015

    DELTA SHUNT KIT, REGULAR, PERFORMANCE LEVEL 1.5

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·April 11, 2013

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 15, 2011

    CLINICAL CHEMISTRY BILIRUBIN CALIBRATOR

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JIX·June 12, 2008

    BD ANGIOCATH¿ IV CATHETER 22G X 1.16 IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·October 31, 2017

    BD ANGIOCATH¿ IV CATHETER 22G X 1.16 IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·August 30, 2017

    EVIS LUCERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDT·August 7, 2023

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·March 17, 2025