BEUDAMED
    28 results · 17ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    ZSFab Lumbar Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus

    FDA Pre-Market Approval
    FDA Class 2 ·COBAS AMPLIPREP/COBAS AMPLICOR HCV TEST V2.0

    Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus

    FDA Pre-Market Approval
    FDA Class 2 ·COBAS AMPLIPREP/COBAS TAQMAN HCV TEST

    Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus

    FDA Pre-Market Approval
    FDA Class 2 ·AMPLICOR HCV TEST V2.0/COBAS AMPLICOR HCV TEST V2.0

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·Artus CMV RGQ and QS-RGQ MDx Kit

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·artus CMV RGQ MDx Kit and artus CMV QS-RGQ MDx Kit

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·artus CMV RGQ MDx Kit and artus CMV QS-RGO MDx Kit

    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·OSTEOSPACE