BEUDAMED
    27 results · 42ms · Sources: EU EUDAMED, US FDA

    Admiral

    FDA UDI
    SEASPINE ORTHOPEDICS CORPORATION·10889981277390·Trial Drill Guide, 25/25 Deg, 10mm

    Helios Dura Regeneration Matrix

    FDA registration
    HELIOS BIOMEDICAL INC.·1 product·🇺🇸 United States

    RESTORIS POROUS PARTIAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HES ULTRASONIC THERAPY APPLIANCE, MODELS HS-3008 (1MHZ), HS3026 (2MHZ), HS-3040 (3MHZ)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Catheter, Percutaneous

    FDA classification
    FDA Class 2 ·Catheter, Percutaneous

    Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

    FDA classification
    FDA Class 2 ·Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

    Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer

    FDA classification
    FDA Class 2 ·Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer