BEUDAMED
    21 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    QUADRA ASSURA MP ICD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·June 3, 2016

    QUADRA ASSURA MP ICD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·June 22, 2016

    UNIFY ASSURA ICD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·March 15, 2017

    UNIFY ASSURA ICD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC·Product code NIK·January 10, 2017

    GALLANT HF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NIK·February 20, 2023

    UNIFY ASSURA DDQP+

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·November 16, 2015

    UNIFY QUADRA MP ICD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code NIK·January 13, 2017

    QUADRA ASSURA DDQP+

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NIK·November 22, 2017

    UNIFY ASSURA DDQP+

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·June 28, 2016

    GALLANT HF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NIK·May 30, 2023

    QUADRA ASSURA MP ICD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·February 9, 2018

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code OJX·May 7, 2022

    QUADRA ASSURA DDQP+

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NIK·August 16, 2018

    QUICKSITE LV

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVY·January 28, 2020

    PRODISC-L INF-PL SIZ L 0°

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code MJO·April 2, 2013

    ONE TOUCH LANCING DEVICE

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·March 25, 2011

    EEA 31MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·April 15, 2008

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 25, 2012

    FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·April 2, 2020

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·November 16, 2011