BEUDAMED
    9 results · 18ms · 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.

    CLINIJEL

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970581·anteriors; shade A2 light; mould CM

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111345579·SPATULA W/ROUND END 4MM

    SILVER ALGINATE II WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    Mako Total Knee Application

    FDA 510(k)
    FDA Class 2 ·Neurology

    RUSCH GREEN RUSCHLITE DISP MTL MILL 2

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code CCW·June 2, 2014

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·February 20, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·January 25, 2011

    CERAMIC ELECTRODE TIP L-HK F/GK372R

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code GEI·July 5, 2019