BEUDAMED
    10 results · 41ms · Sources: EU EUDAMED, US FDA
    Filters FDA Classification ×

    Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness

    FDA classification
    FDA Class 2 ·Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA classification
    FDA Class 2 ·Cytomegalovirus (Cmv) Dna Quantitative Assay

    Test, Donor, Cmv

    FDA classification
    FDA Class 2 ·Test, Donor, Cmv

    Multiplex Flow Immunoassay, T. Gondii, Rubella And Cmv

    FDA classification
    FDA Class 2 ·Multiplex Flow Immunoassay, T. Gondii, Rubella And Cmv

    Attachment, Intermittent Mandatory Ventilation (Imv)

    FDA classification
    FDA Class 2 ·Attachment, Intermittent Mandatory Ventilation (Imv)

    Qualitative Cytomegalovirus Nucleic Acid-Based Detection Device For Congenital Cytomegalovirus Infection

    FDA classification
    FDA Class 2 ·Qualitative Cytomegalovirus Nucleic Acid-Based Detection Device For Congenital Cytomegalovirus Infection

    Ultrasonic Body Composition Analyzer

    FDA classification
    FDA Class 2 ·Ultrasonic Body Composition Analyzer

    Filler, Bone Void, Calcium Compound

    FDA classification
    FDA Class 2 ·Filler, Bone Void, Calcium Compound

    Multiplex Immunoassay For T. Gondii, Rubella, Cytomegalovirus And Herpes Simplex Virus 1 And 2

    FDA classification
    FDA Class 2 ·Multiplex Immunoassay For T. Gondii, Rubella, Cytomegalovirus And Herpes Simplex Virus 1 And 2

    Multiplex Flow Immunoassay, T. Gondii, Rubella, Cmv Igm

    FDA classification
    FDA Class 2 ·Multiplex Flow Immunoassay, T. Gondii, Rubella, Cmv Igm