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

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    Filters FDA Adverse Event ×

    FRX DEFIBRILLATOR, ITALIAN, EXCHANGE

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MKJ·March 15, 2022

    FRX (W B) DEFIB, THAI, EXCHG

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MKJ·March 15, 2022

    HEARTSTART FRX DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MKJ·May 26, 2022

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·October 31, 2012

    FRESENIUS 2008K

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·April 25, 2014

    VERSAPOINT

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HIH·August 12, 2010

    ABSOLUTE PRO VASCULAR SELF-EXPANDING STENT SYSTEM

    FDA Adverse Event
    Death ·ABBOTT VASCULAR·Product code FGE·July 21, 2020

    ABSOLUTE PRO VASCULAR SELF-EXPANDING STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code FGE·February 27, 2020

    CSF-FLOW CONTROL SHUNT KIT CONTOURED REGULAR, MEDIUM PRESSURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·March 11, 2019

    ABSOLUTE PRO VASCULAR SELF-EXPANDING STENT SYSTEM

    FDA Adverse Event
    Death ·ABBOTT VASCULAR·Product code FGE·February 27, 2020