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

    TPH TECHNOLOGY MALAYSIA SDN. BHD.

    FDA registration
    TPH TECHNOLOGY MALAYSIA SDN. BHD.·1 product·🇲🇾 Malaysia

    eufy Wearable Breast Pump S1 (T8D02);

    FDA registration
    SHENZHEN TPH TECHNOLOGY CO., LTD.·1 product·🇨🇳 China

    eufy Wearable Breast Pump S1 (T8D02) Model T8D02; eufy Wearable Breast Pump E10 (T8D03) Model T8D03; eufy Wearable Breast Pump S1 Pro (T8D04) Model T8D04; eufy Wearable Breast Pump E20 (T6060) Model T6060;

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Pump, Breast, Powered

    FDA classification
    FDA Class 2 ·Pump, Breast, Powered

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690124788·Modular Stem 15mm x 125mm

    R1 shock-proof black, 1-tube, disinfectable one-piece cuff, obese size

    FDA UDI
    Rudolf Riester GmbH·04045396178458·Aneroid sphygmomanometers for non invasive meas...

    Octance Straight PC

    FDA registration
    Choice Spine·1 product·🇺🇸 United States

    Octane Straight / IR PC

    FDA registration
    Sterigenics U.S., LLC·1 product·🇺🇸 United States

    Octane™ Straight Intervertebral Fusion Device, Ti Coated

    FDA registration
    EAGLE MEDICAL PACKAGING STERILIZATION, INC.·1 product·🇺🇸 United States

    Eagle1350 (NT,SN) - Octane Straight Intervertebral Fusion Device, Ti Coated

    FDA registration
    ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

    Octane Straight PC

    FDA registration
    EXACTECH, INC.·1 product·🇺🇸 United States

    PALM PRO

    FDA registration
    DIPPED PRODUCTS (THAILAND) LTD·1 product·🇹🇭 Thailand

    Eagle1350 (NT,SN) - Octane Straight Intervertebral Fusion Device, Ti Coated

    FDA registration
    Isomedix Operations, Inc·1 product·🇺🇸 United States

    Neu Platform

    FDA registration
    NEUHEALTH DIGITAL LTD·1 product·🇬🇧 United Kingdom

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210152111·Resolve® Ceramic R022 UL 5-5 CS BC HK

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210152811·Resolve® Ceramic M022 UL 5-5 CS BC HK

    Resolve® Ceramic

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K210152121·Resolve® Ceramic R022 UL 5-5 CS HK/MBT 4-5

    PALM PRO PREMIUM, MODEL 6PF1 & PALM PRO, MODEL 6PF2, LATEX EXAM GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    The Octane Straight Intervertebral Fusion Device, Ti Coated

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar