BEUDAMED
    13 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·July 30, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·December 16, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·April 21, 2016

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·April 21, 2016

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·May 13, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·May 13, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·June 8, 2017

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·November 11, 2015

    DIAMONDTEMP ABLATION SYSTEM

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

    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