BEUDAMED
    4 results · 21ms · 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 ×

    EVOLVE

    FDA Adverse Event
    Malfunction ·ARJOHUTNLEIGH, INC.·Product code IKY·May 2, 2014

    OT ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 7, 2013

    MERIT CUSTOM KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·October 23, 2010

    FEMORAL MODULAR HEAD - S Ø28MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LPH·April 13, 2023