BEUDAMED
    8 results · 28ms · 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 ×

    0.015CC PINPOINT IONIZATION CHAMBER, 0.005 CC PINPOINT IONIZATION CHAMBER

    FDA 510(k)
    FDA Class 2 ·Radiology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972212·posteriors; shade A3 light; size L; upper jaw

    SCHWERT

    FDA UDI
    A. Schweickhardt GmbH & Co. KG·E89649722120·Impr.trays perforated Inf BU B2

    MATISSE Anterior Cervical Interbody Fusion Cage System, Ti-PEEK™

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JET-X BAR SYSTEM CLAMPS, BARS AND POSTS-MR SAFE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARCHITECT HBSAG QUALITATIVE II REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND·Product code KSJ·February 21, 2013

    IUNI G2

    FDA Adverse Event
    Injury ·CONFORMIS·Product code HSX·January 18, 2011

    UNKNOWN DEPUY SZ 4 12.5 CURVED TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·July 31, 2014