BEUDAMED
    8 results · 17ms · 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.

    MAGNETRON MUNICH MODEL ELECTRONIC CONTROL UNIT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Snowden-Pencer

    FDA UDI
    STERIS CORPORATION·10885403183287·DIAMOND-FLEX 40 DEG ARTICULATING FORCEPS MARYLA...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197959·AK3 PS-C Insert Trial Size 5, 11mm

    ELECATH PERCUTANEOUS LEFT ATRIAL CANNULATION SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TDX TOTAL ESTRIOL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·June 25, 2014

    OASYS ADJUSTABLE DRILL GUIDE

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code DZJ·December 27, 2012

    MYNX VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·November 9, 2010