BEUDAMED
    59 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SYSTEM98

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·June 19, 2014

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 26, 2013

    1 MM SCREW 1.0MM X 3.0MM

    FDA Adverse Event
    BIOMET MICROFIXATION·Product code HWC·May 24, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·August 5, 2008

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·December 22, 2011

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·May 23, 2013

    ENDURANT II ILIAC STENT GRAFT

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·May 19, 2021

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·May 10, 2012

    COBAS 4800 HPV TEST

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS·Product code MAQ·July 17, 2017

    COBAS 4800 HPV TEST, CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MAQ·May 10, 2012

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC ATS 3F THERAPEUTICS·Product code LWR·June 8, 2012

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC ATS 3F THERAPEUTICS·Product code LWR·May 10, 2012

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVE DIVISION·Product code LWR·November 11, 2021

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·April 26, 2021

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·April 26, 2021

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVE DIVISION·Product code LWR·May 19, 2021

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC 3F THERAPEUTICS, INC.·Product code LWR·November 21, 2018

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·October 29, 2018

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC 3F THERAPEUTICS, INC.·Product code LWR·November 13, 2025

    THV 1000-23 3F AORTIC BIO 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC 3F THERAPEUTICS, INC.·Product code LWR·October 15, 2025