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

    D-T099KW, D-T012, D-T012W

    FDA registration
    SHENZHEN BEAUTY EVERY MOMENT INTELLIGENT ELECTRIC CO.,LTD.·1 product·🇨🇳 China

    IPL Home Use Hair Removal Device, Model: D-T019

    FDA registration
    LIFESTYLES HEALTH PRODUCTS CO., LTD.·1 product·🇨🇳 China

    IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W)

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

    Light Based Over-The-Counter Hair Removal

    FDA classification
    FDA Class 2 ·Light Based Over-The-Counter Hair Removal

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319707654·St. Mark's Deep Pelvic Retractor, hollow handle...

    CD Horizon Legacy 6.35 Ti

    FDA registration
    Medtronic Medical Costa Rica S.R.L.·5 products·🇨🇷 Costa Rica

    CD Horizon Legacy 6.35 Ti

    FDA registration
    MEDTRONIC SOFAMOR DANEK USA, INC.·5 products·🇺🇸 United States

    GRANDWAY TECHNOLOGY (SHENZHEN) LIMITED

    FDA registration
    GRANDWAY TECHNOLOGY (SHENZHEN) LIMITED·1 product·🇨🇳 China

    CD Horizon Legacy 6.35 Ti

    FDA registration
    MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO·5 products·🇺🇸 United States

    CD Horizon Legacy 6.35 Ti

    FDA registration
    Medtronic Engineering and Innovation Center (MEIC)·5 products·🇮🇳 India

    CD Horizon Legacy 6.35 Ti

    FDA registration
    WARSAW ORTHOPEDIC, INC.·5 products·🇺🇸 United States

    VitaVitro® Single Lumen Oocyte Retrieval Needle

    FDA registration
    Shenzhen VitaVitro Biotech Co.,Ltd.·1 product·🇨🇳 China

    iTero Lumina Pro

    FDA registration
    Align Technology, Ltd.·2 products·🇮🇱 Israel

    iTero Lumina Pro

    FDA registration
    Aligntech de Mexico S, de R. L. de C. V.·2 products·🇲🇽 Mexico

    MODIFICATION TO: CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIGITAL AUTOMATIC BLOOD PRESSURE MONITOR BPM20 SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Orthosis, Spinal Pedicle Fixation

    FDA classification
    FDA Class 2 ·Orthosis, Spinal Pedicle Fixation

    System, Measurement, Blood-Pressure, Non-Invasive

    FDA classification
    FDA Class 2 ·System, Measurement, Blood-Pressure, Non-Invasive