BEUDAMED
    72 results · 36ms · 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

    ELLIPSE DR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 2, 2013

    INSORB SUBCUTICULAR STAPLER

    FDA Adverse Event
    INCISIVE SURGICAL, INC.·Product code GDW·September 8, 2014

    PRODISC-L POLYETHYLENE INLAY

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MJO·May 6, 2011

    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

    DIAMONDTEMP ABLATION SYSTEM

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

    E-LUMINEXX VASCULAR STENT

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

    SEE H10

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