BEUDAMED
    8 results · 20ms · 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 ×

    BANDTITE GLASS IONOMER CEMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756666046·ADULT/PEDS SUTURE LACERATION TRAY

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471149892·K-WIRE - DOUBLE TROCAR FULLY THREADED 2.4mm DIA...

    VERIMED MYOEXORCISER III (MYO III)

    FDA 510(k)
    FDA Class 2 ·Neurology

    BEHIND-THE-EAR HEARING AID MODEL 303 ASP

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    NEUROPORT ARRAY

    FDA Adverse Event
    Injury ·BLACKROCK MICROSYSTEMS·Product code GZL·June 20, 2014

    ACCENT SR RF OUS

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·November 10, 2010

    6600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 5, 2012