BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    DIAMONDTEMP ABLATION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code OAE·August 9, 2023

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·April 16, 2013

    VITALITY 2

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

    SEE H10

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·March 4, 2019

    BD INSULIN PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2015

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·January 3, 2013

    UNKNOWN CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC DOMINICANA·Product code JXG·December 17, 2025

    TACTICATH¿ CONTACT FORCE ABLATION CATHETER, SENSOR ENABLED¿

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code OAE·May 4, 2023

    EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDA·February 18, 2026

    REPLACEMENT HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·April 20, 2018