BEUDAMED
    8 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