BEUDAMED
    2 results · 68ms · Sources: EU EUDAMED, US FDA
    Filters FDA FEI Number: 3003186357 ×

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·Minitouch 3.8 Era System (Minitouch System)

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·Minitouch 3.8 Era System (Minitouch System)