BEUDAMED
    3 results · 26ms · 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 ×

    ADULT CPB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DWF·March 14, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2015

    OT METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·September 23, 2010