BEUDAMED
    6 results · 19ms · 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 Regulation: Us FDA ×

    ALPHA-DENT LIGHT ACTIVATED CORE BUILDUP BLUE PASTE

    FDA 510(k)
    FDA Class 2 ·Dental

    SMITH & NEPHEW VARIABLE-ANGLE LOCKING MINI-FRAGMENT PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIAMOND SETUP 2000

    FDA 510(k)
    FDA Class 2 ·Radiology

    HOSPIRA PRIMARY PLUMSET

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FPA·January 22, 2013

    FIRE STAR RX PTCA BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code LOX·December 20, 2010

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 14, 2014