BEUDAMED
    20 results · 7ms · Sources: EU EUDAMED, US FDA

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

    Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

    FDA classification
    FDA Class 2 ·Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

    ORGENTEC ANTI-SS-A(RO) ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    AUTOSTAT II ANTI-SS-A/RO ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    IMMUNOWELL SJOGRENS SYNDROME A (RO)ANTIBODY TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    RHEUMELISA ASSAY FOR SS-A/RO AUTOANTIBODIES

    FDA 510(k)
    FDA Class 2 ·Immunology

    ANTI-ENA ANTIBODY TEST [SS-A (RO)]

    FDA 510(k)
    FDA Class 2 ·Immunology

    ORGENTEC ANTI-SS-A(RO) PIN IMMUNO ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    ENZYME IMMUNOASSAY ANTI-SS-A/RO ANTIBODY TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    SS-A(RO) & SS-B(LA) ANTIBODY ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    ANTI-SS-A (RO) AND ANTI-SS-B (LA) ANTIBODY TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    ENAII TEST KIT(SS-A(RO) & SS-B(LA) AUTOANTIBODY

    FDA 510(k)
    FDA Class 2 ·Immunology

    RELSIA SS-A/RO & SS/B LA ANTIBODY TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    ImmuLisa Enhanced SS-A (Ro) Antibody ELISA, ImmuLisa Enhanced SS-B (La) Antibody ELISA, ImmuLisa Enhanced Sm Antibody ELISA, ImmuLisa Enhanced RNP Antibody ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    Sterilizer, Dry Heat

    FDA classification
    FDA Class 2 ·Sterilizer, Dry Heat

    Igm (Mu Chain Specific), Antigen, Antiserum, Control

    FDA classification
    FDA Class 2 ·Igm (Mu Chain Specific), Antigen, Antiserum, Control

    Device, Fluidized Therapy, Dry Heat

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

    Di (O-Hydroxyphenylimine) Ethane, Calcium

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

    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