BEUDAMED
    8 results · 26ms · 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.

    TYPE 9541 RECORDER, PAPER CHART

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197270·AK3 PS-R Insert Trial Size 1, 11mm

    CHARTER HARD CONTACT LENS CLEANING SOLUTION

    FDA 510(k)
    FDA Unclassified ·Unknown

    DISPOSABLE PLASTIC DENT IMPRESSION TRAYS 9 STYLES

    FDA 510(k)
    FDA Class 2 ·Dental

    GIALLOY CB BLANK

    FDA UDI
    SRL Dental GmbH·ESRL58951111·Aufbrennfähige Nichtedelmetall-Dental-Fräslegie...

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 25, 2014

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·November 10, 2010

    OT VERIO METER

    FDA Adverse Event
    LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 3, 2013