BEUDAMED
    11 results · 42ms · Sources: EU EUDAMED, US FDA
    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

    Board, Bed

    FDA classification
    FDA Class 1 ·Board, Bed

    Electrocardiograph

    FDA classification
    FDA Class 2 ·Electrocardiograph

    Hiv-1 Genotyping Assay Using Ngs Technology

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

    Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    FDA classification
    FDA Class 3 ·Next Generation Sequencing Oncology Panel, Somatic Or Germline Variant Detection System

    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

    Dna And Rna Oncology Controls

    FDA classification
    FDA Class 2 ·Dna And Rna Oncology Controls

    Tympanometer, Exempt

    FDA classification
    FDA Class 2 ·Tympanometer, Exempt

    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