BEUDAMED
    7 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.
    Filters Regulation: Us FDA ×

    INTEGRATED VISUALIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970598·anteriors; shade A2 light; mould ITS

    ZeroWire Mobile

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNIDENTIFIED DEPUY STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC·Product code KWA·February 20, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 25, 2011

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·July 31, 2014