BEUDAMED
    15 results · 40ms · 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 Status: Other ×

    BOOMERANG

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code DXC·May 21, 2007

    BOOMERANG

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·April 11, 2007

    BOOMERANG

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·March 5, 2007

    BOOMERANG

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·March 16, 2007

    BOOMERANG 610

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·February 9, 2007

    BOOMERANG 610

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·February 20, 2007

    BOOMERANG 610

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·February 20, 2007

    BOOMERANG 610

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·January 24, 2006

    BOOMERANG 610

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·February 14, 2006

    BOOMERANG 56

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·December 9, 2005

    BOOMERANG 610

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·December 29, 2005

    BOOMERANG 56

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·December 5, 2005

    BOOMERANG 610

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·December 16, 2006

    VASCADE VCS CLOSURE DEVICE

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·May 16, 2025

    BOOMERANG

    FDA Adverse Event
    Other ·CARDIVA MEDICAL, INC.·Product code MGB·August 10, 2006