BEUDAMED
    28 results · 46ms · Sources: EU EUDAMED, US FDA

    DEEPVESSEL FFR

    FDA registration
    KEYA MEDICAL TECHNOLOGY CO.,LTD.·1 product·🇨🇳 China

    ViSi Mobile Monitoring System

    FDA registration
    SOTERA WIRELESS·1 product·🇺🇸 United States

    Pro-Nox

    FDA registration
    Laser Marketing Group, LLC·1 product·🇺🇸 United States

    MODIFICATION TO: BIOMET HUMERAL CABLE PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SAPPHIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

    FDA classification
    FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA classification
    FDA Class 2 ·Catheters, Transluminal Coronary Angioplasty, Percutaneous

    Plate, Fixation, Bone

    FDA classification
    FDA Class 2 ·Plate, Fixation, Bone