BEUDAMED
    4 results · 32ms · Sources: EU EUDAMED, US FDA

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    Exodus Revision

    FDA UDI
    Tightline Development, LLC·00850019455052·

    Exodus Revision

    FDA UDI
    Tightline Development, LLC·00850019455717·

    BULK NON STER XCOAT DELPH PUMP

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·October 15, 2015

    FUSED LIGHT CABLE, 5.0 MM X 274CM (9.0')

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code FST·July 1, 2020