BEUDAMED
    4 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CA-1000

    FDA Adverse Event
    Injury ·TOA MEDICAL ELECTRONICS·Product code GKP·January 6, 1997

    FLEXI-SEAL FMS

    FDA Adverse Event
    Injury ·CONVATEC·Product code KNT·November 29, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 5, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 20, 2012