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

    Intranasal Electrostimulation Device For Dry Eye Symptoms

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

    Antisera, Cf, Equine Encephalitis Virus, Eee, Wee

    FDA classification
    FDA Class 1 ·Antisera, Cf, Equine Encephalitis Virus, Eee, Wee

    Intense Pulsed Light Device For Managing Dry Eye

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

    Gases Used Within Eye To Place Pressure On Detached Retina

    FDA classification
    FDA Class 3 ·Gases Used Within Eye To Place Pressure On Detached Retina

    Antigens, Cf (Including Cf Control), Equine Encephalitis Virus, Eee, Wee

    FDA classification
    FDA Class 1 ·Antigens, Cf (Including Cf Control), Equine Encephalitis Virus, Eee, Wee

    Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

    FDA classification
    FDA Class 1 ·Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

    Media, Culture, Ex Vivo, Tissue And Cell

    FDA classification
    FDA Class 2 ·Media, Culture, Ex Vivo, Tissue And Cell