BEUDAMED
    5 results · 17ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Injury ×

    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

    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