BEUDAMED
    4 results · 36ms · 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 ×

    ARGYLE SALEM SUMP TUBE WITH ANTI-REFLUX VALVE

    FDA Adverse Event
    Malfunction ·SHERWOOD DAVIS AND GECK·Product code KNT·August 29, 1996

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·May 6, 2014

    NEURON DELIVERY CATHETER 053

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·March 15, 2010

    MARYLAND BIPOLAR FORCEPS

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·November 13, 2012