BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARTiC-L 3D Ti Spinal System with TiONIC Technology, ARTiC-XL 3D Ti Spinal System with TiONIC Technology

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LECTRAJET NEEDLE-FREE INJECTION SYSTEM, MODEL: M3 RA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Wire, Guide, Catheter

    FDA classification
    FDA Class 2 ·Wire, Guide, Catheter

    Injector, Fluid, Non-Electrically Powered

    FDA classification
    FDA Class 2 ·Injector, Fluid, Non-Electrically Powered

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar