BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Classification ×

    Tricuspid Valve Repair Device, Percutaneously Delivered

    FDA classification
    FDA Class 3 ·Tricuspid Valve Repair Device, Percutaneously Delivered

    Ldt, Approved By Nys Clep

    FDA classification
    FDA Not Classified ·Ldt, Approved By Nys Clep

    Electrocardiograph

    FDA classification
    FDA Class 2 ·Electrocardiograph

    Board, Bed

    FDA classification
    FDA Class 1 ·Board, Bed

    Hiv-1 Genotyping Assay Using Ngs Technology

    FDA classification
    FDA Class 2 ·Hiv-1 Genotyping Assay Using Ngs Technology

    Ngs Whole Genome Sequencing For Sars-Cov-2 Genetic Analysis

    FDA classification
    FDA Not Classified ·Ngs Whole Genome Sequencing For Sars-Cov-2 Genetic Analysis

    Serology Test Used For Screening Of Cadaveric (Non-Heart-Beating) Donors Of Blood Or Blood Products Or Hct/Ps

    FDA classification
    FDA Unclassified ·Serology Test Used For Screening Of Cadaveric (Non-Heart-Beating) Donors Of Blood Or Blood Products Or Hct/Ps

    Nucleic Acid Test Used For Screening Of Cadaveric (Non-Heart-Beating) Donors Of Blood Or Blood Products Or Hct/Ps

    FDA classification
    FDA Unclassified ·Nucleic Acid Test Used For Screening Of Cadaveric (Non-Heart-Beating) Donors Of Blood Or Blood Products Or Hct/Ps