BEUDAMED
    14 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    FORTIFY ASSURA DR ICD, US

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·June 13, 2016

    FORTIFY ASSURA VR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

    ELLIPSE VR ICD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

    CD2257-40Q FORTIFY ASSURA DR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVZ·June 14, 2017

    FORTIFY ASSURA VR ICD_IDE_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code NVZ·October 31, 2017

    UNIFY ASSURA CRT-D RF HV

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·March 29, 2019

    FORTIFY ST DR, U1.6 SJ4 ID

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·January 18, 2017

    FORTIFYASSURA DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 3, 2017

    FORTIFY ASSURA VR ICD_O_US

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 27, 2016

    CONTOUR II V-185 AC SERIES TIERED THERAPY DEFIB

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·November 26, 1999

    SPINAL NEEDLE 25GA 3.50 IN FOR INDIA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·November 13, 2020

    SARA 3000

    FDA Adverse Event
    Other ·ARJOHUNTLEIGH POLSKA SP. Z O.O.·Product code FSA·November 12, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 10, 2010

    PUREPOINT

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQF·February 25, 2014