Recently, Kossel Medtech’s independently developed Sabelly® non-compliant peripheral balloon dilatation catheter has received approval for market release from the National Medical Products Administration (NMPA).

The Sabelly® non-compliant peripheral balloon dilatation catheter is designed for percutaneous intravascular angioplasty within the peripheral vascular system, including the dilation of the iliac arteries, veins, upper and lower vena cava, and abdominal aorta. As the first domestically produced large-diameter balloon catheter to receive market approval, it contributes to breaking the monopoly of imported products in the domestic market.

With a balloon diameter of up to 30mm, the Sabelly® non-compliant peripheral balloon dilatation catheter is designed to meet clinical needs and offers advantages such as good passability and stable deliverability. This product performs exceptionally well in treating larger-diameter venous stenotic lesions, including pre-dilation and post-dilation of iliac veins, and undoubtedly provides a more ideal choice for clinical applications.