BEUDAMED
    2,871 results · 66ms · Sources: EU EUDAMED, US FDA

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·GENESIS AND EON FAMILY NEUROSTIMULATION (IPG) SYSTEMS

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·EON MINI, PRODIGY AND BRIO CHARGING SYSTEMS

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·GENESIS AND EON FAMILY NEUROSTIMULATION (IPG) SYSTEMS

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·GENESIS AND EON FAMILY NEUROSTIMULATION (IPG) SYSTEMS

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·GENESIS AND EON FAMILY NEUROSTIMULATION (IPG) SYSTEMS

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·Eon Mini™ IPG, 16-Channel Rechargeable; Prodigy MRI IPG; Protégé IPG; Protégé MRI IPG; Eon Patient Programmer; Patient P

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·GENESIS, GENESIS RC AND THE EON NEUROSTIMULATION SYSTEMS

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·GENESIS, GENESIS RC AND THE EON NEUROSTIMULATION SYSTEMS

    FUSION-DOE

    FDA registration
    DENTLIGHT INC.·2 products·🇺🇸 United States

    LED Curing Lights; DB686 HALO

    FDA registration
    FOSHAN COXO MEDICAL INSTRUMENT CO., LTD.·2 products·🇨🇳 China

    LumiCare

    FDA registration
    GreenMark Biomedical Lab·2 products·🇺🇸 United States

    BioLyse-EO-1 MN53

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·Bioxol Kft·2 devices

    BioLyse-EO-2 MN53

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·Bioxol Kft·2 devices

    BioLyse-EO-1 MN5

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·Bioxol Kft·2 devices

    BioLyse-EO-2 MN5

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·Bioxol Kft·2 devices

    HAIRMAX DUAL 12

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SERVOTRONIC EC100 SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    CARETONE II

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    S-ROM FEMORAL HIP STEM(SIZES 12 X 06 X 115 AND 12 X 07 X 115)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TANTHERA-T35

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery