BEUDAMED
    6 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 ×

    NEBULIZER (DIRECT PATIENT INTERFACE)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    COLOSCREEN

    FDA 510(k)
    FDA Class 2 ·Hematology

    SPECIFIC ALLERGEN MODULES FOR ALASTAT ALLERGEN IGE

    FDA 510(k)
    FDA Class 2 ·Immunology

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·November 17, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 7, 2014

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Malfunction ·OPTONOL, LTD·Product code KYF·December 20, 2012