BEUDAMED
    4 results · 15ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    VIASYS

    FDA Adverse Event
    Malfunction ·CAREFUSION 207, INC·Product code CBK·October 26, 2009

    ULTRASLIDE

    FDA Adverse Event
    Malfunction ·SKYTRON·Product code GDC·March 25, 2013

    SOFTCLIX LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·April 1, 2008

    COLUMBUS UCR TIBIAL PLATEAU CEMENTED T2+

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code JHW·July 24, 2015