BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE

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

    Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

    FDA classification
    FDA Class 2 ·Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

    ASSUFIL

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

    NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    Stimulator, Neuromuscular, External Functional

    FDA classification
    FDA Class 2 ·Stimulator, Neuromuscular, External Functional

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA classification
    FDA Class 2 ·Suture, Absorbable, Synthetic, Polyglycolic Acid