Genesis MedTech products

Safe and Reliable: Unique silicone material, high thermal resistance, with high temperature resistance above 300 ?. Better device insertion force and air tightness, stable and comfortable operation.

stapling system now re-imagined and reassembled into a brand-new entity. Signature tissue compression paired with smooth powered firing yields unprecedented experience, unlocking new possibilities in the OR.

ArtiSential`s double-jointed end-effector enables precise access to complex, difficult- to-reach surgical spaces.

The absorbable single-strand suture of polydioxanone (PDO) can support the wound for more than 6 weeks, with little tissue reaction and no foreign body residue. The tension attenuation of PDO material is not affected by the alkaline environment of pancreatic juice and bile, proving it to be remarkable safe. The monofilament structure of PDO suture has a smooth, round surface with strong penetrability that can penetrate the tissue smoothly, with little damage to the body. The bacterial colonization of single-strand sutures is significantly lower than that of braided sutures, reducing the incidence of SSI.

Fast-absorbing products are made of specially treated polyglycolic acid (PGA) and woven with multiple sterile strands. Suitable for superficial soft tissue, such as skin and mucous membranes or other short-term wound support.

No damage to blood vessels, operation is more secure.

The Chocolate Touch drug-coated balloon is the world’s first balloon catheter that combines therapeutic agent delivery with the next generation of controlled dilation angioplasty technique, for the treatment of peripheral vascular diseases. It is designed with the aim to provide patients suffering from peripheral vascular disease with a safer and more effective treatment than traditional balloon angioplasty.

J-Valve system: a new generation TAVI Device with 3 claspers. 3 Claspers deployed at the bottom level of Valsalva sinus.  CValve migrating to the propriate position with guidance of the claspers. DJ-Valve^® self-expanded and system completely deployed. EJ-Valve^® fixed in annulus level and delivery device withdrawed.