BEUDAMED
    4 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 1 ×

    COBAS 4800 CT / NG TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF PROGESTERONE IN SALIVA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Dna Probe, Nucleic Acid Amplification, Chlamydia

    FDA classification
    FDA Class 1 ·Dna Probe, Nucleic Acid Amplification, Chlamydia

    Radioimmunoassay, Progesterone

    FDA classification
    FDA Class 1 ·Radioimmunoassay, Progesterone