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

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

    NICOLET EME LEGEND TC22

    FDA 510(k)
    FDA Class 2 ·Radiology

    EME SELF MONITORING BLOOD GLUCOSE SYSTEM, EME PRO SELF MONITORING BLOOD GLUCOSE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    EME MP3000 MONITORING AND DIAGNOSTIC RESTING ECG

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SAPPHIRE 4ME EMG/EP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    SAPPHIRE SERIES 1P, 1L, 2L, AND 2ME

    FDA 510(k)
    FDA Class 2 ·Neurology

    Eye Tray

    FDA classification
    FDA Class 2 ·Eye Tray

    Coating, Denture Hydrophilic, Resin

    FDA classification
    FDA Class 2 ·Coating, Denture Hydrophilic, Resin

    Implant, Eye Valve

    FDA classification
    FDA Class 2 ·Implant, Eye Valve

    Implant, Eye Sphere

    FDA classification
    FDA Class 2 ·Implant, Eye Sphere

    Monitor, Eye Movement

    FDA classification
    FDA Class 2 ·Monitor, Eye Movement

    Monitor, Eye Movement, Diagnostic

    FDA classification
    FDA Class 2 ·Monitor, Eye Movement, Diagnostic

    Exercise Equipment, Powered, Emg-Triggered

    FDA classification
    FDA Class 2 ·Exercise Equipment, Powered, Emg-Triggered

    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