BEUDAMED
    9,478 results · 45ms · Sources: EU EUDAMED, US FDA

    GlucoLeader

    Basic UDI-DI
    EU IVDD · Eu Ivd Annex 2 List B ·HMD Biomedical Inc.·1 device

    GlucoLeader

    Basic UDI-DI
    EU IVDD · Eu Ivd Annex 2 List B ·HMD Biomedical Inc.·1 device

    GlucoLeader

    Basic UDI-DI
    EU IVDD · Eu Ivd Annex 2 List B ·HMD Biomedical Inc.·1 device

    GlucoLeader

    Basic UDI-DI
    EU IVDD · Eu Ivd Annex 2 List B ·HMD Biomedical Inc.·1 device

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·COFLEX® INTERLAMINAR TECHNOLOGY

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·COFLEX INTERLAMINAR TECHNOLOGY

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·COFLEX INTERLAMINAR TECHNOLOGY

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·COFLEX® INTERLAMINAR TECHNOLOGY

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·coflex Interlaminar Stabilization Device

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·COFLEX® INTERLAMINAR TECHNOLOGY

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·coflex® Interlaminar Technology

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·COFLEX® INTERLAMINAR TECHNOLOGY

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·COFLEX® INTERLAMINAR TECHNOLOGY

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·coflex® Interlaminar Technology

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·coflex Interlaminar Stabilization Device

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·coflex Interlaminar Technology

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·Paradigm Spine Coflex Interlaminar Stabilization Device

    Prosthesis, Spinous Process Spacer/Plate

    FDA Pre-Market Approval
    FDA Class 3 ·coflex® Interlaminar Technology

    2MT

    Importer
    🇫🇷 France

    IP85072: Sterile, Single Use, SET AMT 3

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·HASA OPTIX·1 device