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

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    Filters FDA Adverse Event ×

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·June 5, 2025

    COMMON NAME PROSTHESIS, RIB REPLACEMENT

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MDI·April 24, 2014

    COMMON NAME PROSTHESIS, RIB REPLACEMENT

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MDI·April 24, 2014

    COMMON NAME PROSTHESIS, RIB REPLACEMENT

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MDI·April 24, 2014

    CORE SUMEX DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·March 20, 2013

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 10, 2011

    INSYNC MAXIMO

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NIK·March 10, 2008

    UNK SEPS KIT

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·May 3, 2013

    COMMON NAME PROSTHESIS, RIB REPLACEMENT

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MDI·April 24, 2014

    COMMON NAME PROSTHESIS, RIB REPLACEMENT

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MDI·April 24, 2014

    MELODY TRANSCATHETER PULMONARY VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPV·December 22, 2015