BEUDAMED
    12 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·March 13, 2017

    VICTORY XL SR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·April 25, 2016

    VICTORY XL DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·May 11, 2017

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·November 19, 2015

    ACCENT DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWP·September 7, 2018

    ACCENT DR RF

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·March 31, 2017

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 24, 2019

    HELICAL BLADE INSERTER

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code LXH·June 18, 2014

    GOBED II

    FDA Adverse Event
    Other ·STRYKER MEDICAL QUEBEC LP·Product code FNL·October 19, 2010

    ARMADA 14 PTA CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LIT·December 19, 2012

    NEXGEN ROTATING HINGE KNEE ARTICULAR SURFACE WITH HINGE POST EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KRO·August 26, 2016

    NEXGEN ROTATING HINGE KNEE OPTION FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KRO·August 26, 2016