BEUDAMED
    4,863 results · 47ms · Sources: EU EUDAMED, US FDA

    Sterivap HP

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·BMT Medical Technology s.r.o.·1 device

    STERIVAP, STERIVAP HP; SELECTOMAT SL

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·BMT Medical Technology s.r.o.·3 devices

    MAXCEM 2

    FDA 510(k)
    FDA Class 2 ·Dental

    SOOTHE-N-SEAL CANKER SORE RELIEF

    FDA 510(k)
    FDA Class 2 ·Dental

    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