Numeris® Guided Coagulation Device
with VisiTrax®

The Numeris® Guided Coagulation Device with VisiTrax® integrates suction, perfusion, and RF energy to ensure consistent cardiac tissue contact and energy transmission  critical to creating complete linear lesions on a beating heart.

The device is CE Mark approved for the coagulation of cardiac tissue using radiofrequency (RF) energy during cardiac surgery for the treatment of arrhythmias including Atrial Fibrillation (AFIB) or Atrial Flutter (AFL). The indication for use accurately describes the Company’s development effort to design the first epicardial  ablation device for truly minimally invasive procedures. The device was designed to be flexible to allow the device to be positioned gently, under direct endoscopic visibility, throughout the atria. While nContact’s device was designed for the Convergent Procedure,  most ablation designs were not originally designed for atrial fibrillation application but rather adopted for use as best technology available.