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

    CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261

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

    Reprocessed Agilis NxT Steerable Introducer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Reprocessed Catheter Introducer

    FDA classification
    FDA Class 2 ·Reprocessed Catheter Introducer

    Electrosurgical, Cutting & Coagulation & Accessories

    FDA classification
    FDA Class 2 ·Electrosurgical, Cutting & Coagulation & Accessories