BEUDAMED
    21 results · 16ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Classification ×

    Surgical Planning Software For Neurological Stereotaxic Instruments

    FDA classification
    FDA Class 2 ·Surgical Planning Software For Neurological Stereotaxic Instruments

    Dental Navigation System

    FDA classification
    FDA Class 2 ·Dental Navigation System

    Unit, Drying

    FDA classification
    FDA Class 1 ·Unit, Drying

    Artificial Iris

    FDA classification
    FDA Class 3 ·Artificial Iris

    Mri Disposable Kit

    FDA classification
    FDA Class 2 ·Mri Disposable Kit

    Sterilizer, Dry Heat

    FDA classification
    FDA Class 2 ·Sterilizer, Dry Heat

    Lens, Iris Reconstruction

    FDA classification
    FDA Class 3 ·Lens, Iris Reconstruction

    Clip, Iris Retractor

    FDA classification
    FDA Class 1 ·Clip, Iris Retractor

    Button, Iris, Eye, Artificial

    FDA classification
    FDA Class 1 ·Button, Iris, Eye, Artificial

    Sterilizer, Endodontic Dry Heat

    FDA classification
    FDA Class 3 ·Sterilizer, Endodontic Dry Heat

    Dilator, Expansive Iris (Accessory)

    FDA classification
    FDA Class 2 ·Dilator, Expansive Iris (Accessory)

    Monitor, Line Isolation

    FDA classification
    FDA Class 1 ·Monitor, Line Isolation

    Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass

    FDA classification
    FDA Class 2 ·Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass

    Cabinet, Table And Tray, Anesthesia

    FDA classification
    FDA Class 1 ·Cabinet, Table And Tray, Anesthesia

    Device, Fluidized Therapy, Dry Heat

    FDA classification
    FDA Class 2 ·Device, Fluidized Therapy, Dry Heat

    Dry Ash Method, Protein-Bound Iodine

    FDA classification
    FDA Class 1 ·Dry Ash Method, Protein-Bound Iodine

    Intranasal Electrostimulation Device For Dry Eye Symptoms

    FDA classification
    FDA Class 2 ·Intranasal Electrostimulation Device For Dry Eye Symptoms

    Neurological Stereotaxic Instrument, Real-Time Intraoperative Mri

    FDA classification
    FDA Class 2 ·Neurological Stereotaxic Instrument, Real-Time Intraoperative Mri

    Intense Pulsed Light Device For Managing Dry Eye

    FDA classification
    FDA Class 2 ·Intense Pulsed Light Device For Managing Dry Eye

    Light Based Device For Dry Age-Related Macular Degeneration

    FDA classification
    FDA Class 2 ·Light Based Device For Dry Age-Related Macular Degeneration