BEUDAMED
    3 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·May 7, 2014

    LARGE MOD HEAD ADAPT 12/14 +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·February 15, 2013

    PURITAN BENNETT VENTILATOR MODEL 840

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·January 12, 2011