BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    MATRIXRIB FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·October 3, 2016

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·August 26, 2016

    TRAPMATIC SYSTEM SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PINPOINT STEREOTACTIC HEAD AND NECK LOCALIZER

    FDA 510(k)
    FDA Class 2 ·Radiology

    PERIPHERAL NERVE BLOCK SUPPORT TRAY

    FDA Adverse Event
    Malfunction ·I-FLOW, LLC·Product code CAZ·October 1, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 29, 2013

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·June 16, 2011

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 20, 2008

    CONTINUOUS TRAY WITH 100MM NEEDLE, STIMULATING

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code CAZ·October 2, 2014

    CONTINUOUS TRAY WITH 100MM NEEDLE 4IN ECHO NEE

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code CAZ·October 3, 2014

    CONTINUOUS TRAY WITH 100MM NEEDLE, NON STIMULA

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code CAZ·October 1, 2014

    PERIPHERAL NERVE BLOCK SUPPORT TRAY : CONTINUEOUS TRAY 100MM NEEDLE STIMULATING

    FDA Adverse Event
    Malfunction ·HALYARD - IRVINE·Product code CAZ·May 12, 2015

    CONTINUOUS TRAY WITH 100MM NEEDLE STIMULATING & 61CM CATHETER

    FDA Adverse Event
    Malfunction ·HALYARD HEALTH - IRVINE·Product code CAZ·November 8, 2015

    CONTINUOUS TRAY WITH 100MM NEEDLE STIMULATING

    FDA Adverse Event
    Malfunction ·HALYARD - IRVINE·Product code CAZ·July 1, 2015

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·May 21, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·April 17, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER (ISRAEL) LTD.·Product code DQK·December 22, 2016