BEUDAMED
    7 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HEARTSTREAM FR2 WITH AN ECG CABLE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS (HTST)·Product code DPS·March 14, 2012

    IQ200

    FDA Adverse Event
    Malfunction ·IRIS INTERNATIONAL·Product code KQO·July 2, 2015

    HANDLE BATTERY POWERED DRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·July 11, 2024

    GEL-FILL MAMMARY IMPLANT, 260 CC

    FDA Adverse Event
    MCGHAN MEDICAL CORP.·Product code FTR·October 3, 1994

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 11, 2013

    SUBDURAL TUNNELING ICP MONITORING KIT

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES SD·Product code GWM·February 22, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·February 25, 2008