BEUDAMED
    6 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    2520274-2013-01380

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·March 13, 2013

    OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code DTK·February 25, 2011

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 22, 2008

    RESOLUTE ONYX RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·March 2, 2022

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·March 2, 2022

    CNS-6201A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·March 7, 2018