BEUDAMED
    7 results · 27ms · 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.

    PEFECT SHOT

    FDA 510(k)
    FDA Class 1 ·Dental

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972019·posteriors; shade A2; size XS; lower jaw

    AKITA2 APIXNEB

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Brisbane ALIF Device, Gladstone ALIF Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3010593814-2015-00597

    FDA Adverse Event
    Malfunction ·July 14, 2015

    14F X 24CM SPLIT STREAM

    FDA Adverse Event
    Malfunction ·MEDCOMP·Product code MSD·February 15, 2013

    SPINNAKER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code KRA·January 27, 2011