BEUDAMED
    6 results · 23ms · 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 ×

    ARTHROTEK INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CHOLESTECH LIPID MONIT SYST, TOTAL CHOL/TRIG PANEL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    EYEOPENER

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

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 27, 2014

    RSP SHOULDER INSTRUMENT

    FDA Adverse Event
    Malfunction ·ENCORE MEDICAL, L.P.·Product code HTQ·November 23, 2010

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 28, 2013