BEUDAMED
    12 results · 44ms · Sources: EU EUDAMED, US FDA
    Filters FDA Classification ×

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Laser Fax Machine

    FDA classification
    FDA Not Classified ·Laser Fax Machine

    Catheter, Intracardiac Mapping, High-Density Array

    FDA classification
    FDA Class 2 ·Catheter, Intracardiac Mapping, High-Density Array

    Catheter, Intracardiac Mapping, High-Density, Reprocessed

    FDA classification
    FDA Class 2 ·Catheter, Intracardiac Mapping, High-Density, Reprocessed

    Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided

    FDA classification
    FDA Class 3 ·Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided

    Flowmeter, Tube, Thorpe, Back-Pressure Compensated

    FDA classification
    FDA Class 1 ·Flowmeter, Tube, Thorpe, Back-Pressure Compensated

    Fibrinogen And Split Products, Fitc, Antigen, Antiserum, Control

    FDA classification
    FDA Class 2 ·Fibrinogen And Split Products, Fitc, Antigen, Antiserum, Control

    Stent, Coronary

    FDA classification
    FDA Class 3 ·Stent, Coronary

    Mr-Guided Focused Ultrasound System

    FDA classification
    FDA Class 3 ·Mr-Guided Focused Ultrasound System

    Syringe, Balloon Inflation, Exempt

    FDA classification
    FDA Class 2 ·Syringe, Balloon Inflation, Exempt

    Biliary Catheter For Stone Removal That May Also Allow For Irrigation And Contrast Injection

    FDA classification
    FDA Class 2 ·Biliary Catheter For Stone Removal That May Also Allow For Irrigation And Contrast Injection

    Ivd Offered As Ldt, First Marketed Before May 6, 2024, Not Modified Beyond Scope Described In Preamble To Ldt Final Rule

    FDA classification
    FDA Not Classified ·Ivd Offered As Ldt, First Marketed Before May 6, 2024, Not Modified Beyond Scope Described In Preamble To Ldt Final Rule