BEUDAMED
    79 results · 32ms · Sources: EU EUDAMED, US FDA

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    E-LUMINEXX BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code FGE·May 20, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·January 18, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·July 24, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·September 10, 2013

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·February 20, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·January 18, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·April 17, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·February 17, 2014

    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
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·July 28, 2012

    ENERGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 10, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·December 3, 2013

    PROFEMUR(R) Z STEM

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·August 2, 2010

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·May 14, 2014

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·December 16, 2013

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code NIO·November 10, 2010

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code NIO·October 2, 2009

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO.·Product code NIO·May 11, 2009

    E-LUMINEXX VASCULAR STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·August 21, 2014

    HANCOCK

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·January 5, 2021