BEUDAMED
    4 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    KATENA

    FDA Adverse Event
    Other ·Product code HND·February 26, 2009

    2008K HEMODIALYSIS SYS. OLC/DIASAFE PLUS

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·March 27, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 14, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 10, 2015