BEUDAMED
    10,000 results · 100ms · Sources: EU EUDAMED, US FDA

    SPINAL CAGES

    Device
    EU MDD · Eu Md Class 2b ·Tsunami Medical SRL·On the market·15 countries

    SPINAL CAGES

    Device
    EU MDD · Eu Md Class 2b ·Tsunami Medical SRL·On the market·15 countries

    SPINAL CAGES

    Device
    EU MDD · Eu Md Class 2b ·Tsunami Medical SRL·On the market·15 countries

    SPINAL CAGES

    Device
    EU MDD · Eu Md Class 2b ·Tsunami Medical SRL·On the market·15 countries

    SPINAL CAGES

    Device
    EU MDD · Eu Md Class 2b ·Tsunami Medical SRL·On the market·15 countries

    SPINAL CAGES

    Device
    EU MDD · Eu Md Class 2b ·Tsunami Medical SRL·On the market·15 countries

    SPINAL CAGES

    Device
    EU MDD · Eu Md Class 2b ·Tsunami Medical SRL·On the market·15 countries

    SPINAL CAGES

    Device
    EU MDD · Eu Md Class 2b ·Tsunami Medical SRL·On the market·15 countries

    SPINAL CAGES

    Device
    EU MDD · Eu Md Class 2b ·Tsunami Medical SRL·On the market·15 countries

    Compresses de gaze abdominales stériles pour laparotomie 40cm x 50cm 17fils/cm2 6plies double emballage avec lacette sachet de 2 compresses

    Device
    EU MDD · Eu Md Class 2a ·Adhe-Els SA.·On the market·1 country

    Compresses de gaze abdominales stériles pour laparotomie 40cm x 50cm 17fils/cm2 6plies X Ray avec lacette sachet de 2 compresses

    Device
    EU MDD · Eu Md Class 2a ·Adhe-Els SA.·On the market·1 country

    Compresses de gaze abdominales stériles pour laparotomie 40cm x 50cm 17fils/cm2 4plies X Ray avec lacette sachet de 2 compresses

    Device
    EU MDD · Eu Md Class 2a ·Adhe-Els SA.·On the market·1 country

    Hepatitis Viral B Dna Detection

    FDA Pre-Market Approval
    FDA Class 3 ·ABBOTT REALTIME HBV

    Fluorescence In Situ Hybridization, Anaplastic Lymphoma Kinase, Gene Rearrangement

    FDA Pre-Market Approval
    FDA Class 3 ·Vysis ALK Break Apart FISH Probe Kit

    Cytomegalovirus (Cmv) Dna Quantitative Assay

    FDA Pre-Market Approval
    FDA Class 2 ·Alinity m CMV Assay

    Fluorescence In Situ Hybridization, Chromosome 17p Deletion (Tp53)

    FDA Pre-Market Approval
    FDA Class 3 ·Vysis CLL FISH Probe Kit

    Test, Fluorescence In Situ Hybridization (Fish), For Bladder Cancer Detection And Monitoring For Recurrence

    FDA Pre-Market Approval
    FDA Class 3 ·UROVYSION BLADDER CANCER KIT

    Lens, Contact (Polymethylmethacrylate)

    FDA Pre-Market Approval
    FDA Unclassified ·POLYCON CONTACT LENS

    Test, Fluorescence In Situ Hybridization (Fish), For Bladder Cancer Detection And Monitoring For Recurrence

    FDA Pre-Market Approval
    FDA Class 3 ·UROVYSION BLADDER CANCER KIT

    Test, Fluorescence In Situ Hybridization (Fish), For Bladder Cancer Detection And Monitoring For Recurrence

    FDA Pre-Market Approval
    FDA Class 3 ·UROVYSION BLADDER CANCER KIT