BEUDAMED
    7 results · 19ms · 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 ×

    GLANZ CARCINOMA GAUGE, KSEA

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    RST-SANEXAS

    FDA registration
    RST-SANEXAS·3 products·🇺🇸 United States

    CHURCHILL 3-WAY STOPCOCK SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CUI FEATHERED SILICONE MALAR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·February 11, 2013

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 5, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014