BEUDAMED
    6 results · 16ms · 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.

    AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ARGILITE 3

    FDA 510(k)
    FDA Class 2 ·Dental

    SET, ADMINISTRATION INTRAVASCULAR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    XENIUM XPH

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION *USD*·Product code KDI·February 22, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011