BEUDAMED
    6 results · 27ms · 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 ×

    CTF SYSTEMS INC, WHOLE-CORTEX MEG SYSTEM (WITH OPTIONAL EEG SUBSYSTEM)

    FDA 510(k)
    FDA Class 2 ·Neurology

    NUVASIVE HELIX ACP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Altus Spine Titanium Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNICEL® DXC 800 PRO SYNCHRON® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·January 27, 2011

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NIK·July 31, 2014

    PILLING ASPIRATING NEEDLE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GAA·September 29, 2006