BEUDAMED
    12 results · 20ms · 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 ×

    DEPUY MOTECH PROFILE ANTERIOR THORACOLUMBAR PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRESTIGE® LP Cervical Disc System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994714848·INNER SHAFT 6973060 6MM INSERTER US

    artegral HD

    FDA UDI
    Merz Dental GmbH·D7091973060·posteriors; shade B2; size XL; upper jaw

    F&P NivairoTM RT046 Non-Vented Hospital Full Face Mask, Standard Elbow Version

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CALAVIEW (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    TALENT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC CARDIOVASCULAR·Product code MIH·February 21, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 28, 2011

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·August 1, 2014

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code MJO·February 9, 2026

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code MJO·February 8, 2026

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code MJO·November 3, 2020

    PFNA BLADE PERF L95 TAN

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HSB·January 21, 2019