BEUDAMED
    8 results · 18ms · 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.

    TriMemo™ SEMIRIGID ANNULOPLASTY RING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·10840200303832·LIMB HOLDER

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013403832·LIMB HOLDER

    Dentivera Milling Disc

    FDA 510(k)
    FDA Class 2 ·Dental

    SCENARIA View

    FDA 510(k)
    FDA Class 2 ·Radiology

    CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·November 19, 2014

    SOFTCLIX® PLUS GT LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·September 22, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 1, 2013