BEUDAMED
    3 results · 27ms · 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 ×

    PROGRASP (TM) FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 4, 2013

    CRYOVALVE - AORTIC VALVE AND CONDUIT

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MIE·December 30, 2010

    UNKNOWN HIP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·July 17, 2014