BEUDAMED
    10,000 results · 52ms · Sources: EU EUDAMED, US FDA

    TIANamp Stool DNA Kit

    Device
    EU IVDR · Eu Ivd Class A ·Tiangen Biotech (Beijing) Co., Ltd.·On the market

    CNA SUPPLEMENT STAPH/STREP

    Device
    EU IVDR · Eu Ivd Class A ·Laboratorios Conda S.A.·On the market·32 countries

    DNA Fragmentation Quantification Assay

    Device
    EU IVDR · Eu Ivd Class A ·EntroGen, Inc.·On the market·32 countries

    ANA Screen FIA Kit

    Device
    EU IVDD · Eu Ivd General ·Shenzhen Zijian Biotechnology Co., Ltd·On the market

    DS-DNA FIA Kit

    Device
    EU IVDD · Eu Ivd General ·Shenzhen Zijian Biotechnology Co., Ltd·On the market

    COLUMBIA CNA AGAR BASE

    Device
    EU IVDR · Eu Ivd Class A ·Laboratorios Conda S.A.·On the market·32 countries

    COLUMBIA CNA AGAR BASE

    Device
    EU IVDR · Eu Ivd Class A ·Laboratorios Conda S.A.·On the market·32 countries

    TIANamp Micro DNA Kit

    Device
    EU IVDR · Eu Ivd Class A ·Tiangen Biotech (Beijing) Co., Ltd.·On the market

    TIANamp Genomic DNA Kit

    Device
    EU IVDR · Eu Ivd Class A ·Tiangen Biotech (Beijing) Co., Ltd.·On the market

    TIANamp Genomic DNA Kit

    Device
    EU IVDR · Eu Ivd Class A ·Tiangen Biotech (Beijing) Co., Ltd.·On the market

    chemagic DNA Blood200 kit

    Device
    EU IVDR · Eu Ivd Class A ·Wallac Oy·On the market·32 countries

    chemagic DNA CS200 kit

    Device
    EU IVDR · Eu Ivd Class A ·Wallac Oy·On the market·32 countries

    Eonis DNA Extraction kit

    Device
    EU IVDR · Eu Ivd Class A ·Wallac Oy·On the market·32 countries

    DNA Vitamin Stoffwechsel Test

    Device
    EU IVDR · Eu Ivd Class A ·Cerascreen GmbH·On the market·3 countries

    IDS ANA Control Set

    Device
    EU IVDR · Eu Ivd Class B ·Immunodiagnostic Systems Limited·On the market·32 countries

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·DIGENE HYBRID CAPTURE2

    Chromogenic In Situ Hybridization, Nucleic Acid Amplification, Her2/Neu Gene, Breast Cancer

    FDA Pre-Market Approval
    FDA Class 3 ·INFORM HER2 DUAL ISH DNA PROBE COCKTAIL

    ACCUPROBE LISTERIA MONOCYTOGENES CULTURE CONFIRMA.

    FDA 510(k)
    FDA Class 2 ·Microbiology

    AFFIRM/VP IDENT.TEST G.VAGINALIS & T.VAGINALIS

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ACCUPROBE MYCOBACTERIUM KANSASII CULT CONFIRM TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology