BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Classification: FDA Class 2 × Regulation: Us FDA × Clear all

    MR DWI/FLAIR Measurement V1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    COLTENE BRILLIANT D.I. DIRECT INLAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Air Compression Therapy Recovery System (model: MF-AWI, MF-AWI.LED.A-801, MF-AWI.LED.B-801, MF-AWI.OLED.A-601, MF-AWI.LED.A-601, MF-AWI.LED.B-601, MF-AWI.OLED.A-401, MF-AWI.LED.A-401, MF-AWI.LED.B-401)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Sterilizer, Dry Heat

    FDA classification
    FDA Class 2 ·Sterilizer, Dry Heat

    Complement C4, Antigen, Antiserum, Control

    FDA classification
    FDA Class 2 ·Complement C4, Antigen, Antiserum, Control

    Complement C1r, Antigen, Antiserum, Control

    FDA classification
    FDA Class 2 ·Complement C1r, Antigen, Antiserum, Control

    Device, Fluidized Therapy, Dry Heat

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

    Intranasal Electrostimulation Device For Dry Eye Symptoms

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

    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

    Di (O-Hydroxyphenylimine) Ethane, Calcium

    FDA classification
    FDA Class 2 ·Di (O-Hydroxyphenylimine) Ethane, Calcium