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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    LS LF PRIMARY I.V. SET 120IN CONV 0.2MICR

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·June 7, 2013

    BECTON-DICKINSON VISITEC

    FDA Adverse Event
    Injury ·BECTON-DICKINSON·Product code FMI·June 5, 2006

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 15, 2014