BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    EXCELSIOR MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code DQY·April 13, 2010

    NONE

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code LFR·April 17, 2015

    EXCELSIOR MICROCATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code DQY·May 18, 2010

    EXCELSIOR MICROCATHETER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - CORK·Product code DQY·August 2, 2010

    TROCHANTERIC NAIL KIT, TI GAMMA3 Ø11X200MM X 130°

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·March 20, 2013

    NEURON DELIVERY CATHETER 070

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·February 4, 2011

    PULSE GEN

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·March 13, 2008

    ACHIEVE MAPPING CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DRF·April 10, 2019

    FLEXCATH ADVANCE STEERABLE SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·April 10, 2019

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·April 10, 2019

    THORATEC® HEARTMATE II®, SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·July 15, 2025