Address: (Linghao Road) No.2 Street, No.20 Economic Development Zone, Hangzhou
Product features Tip structure-With a tapered smoothtip,Reduce damage to the vessel wall. Hydrophilic coating-Independent research and developmentof hydrophilic coating process, ultra-sliding push. -Reducetransport resistance during operationMake the delivery system more accessibleto the distal......Send Inquiry
Tip structure-With a tapered smooth tip, Reduce damage to the vessel wall.
Hydrophilic coating-Independent research and development of hydrophilic coating process, ultra-sliding push.
-Reduce transport resistance during operation. Make the delivery system more accessible to the distal lesion.
International new materials manufacturing-Pebax semi-compliant balloon material
Fast exchange conveyor system-Easy to control, reduce the operation time, reduce the risk of surgery 750px fast exchange section. Compatible with 0.014 inch microcircuit
Three inner layer tube-Reduce the push resistance of the guide wire and provide support and pressure-bearing
The product is a clinically proven, primary endovascular item for peripheral transluminal angioplasty for peripheral vascular system (including the iliac artery,femoral artery, iliac femoral artery and inferior genicular artery)
Vision & Goal - Barty is committed to becoming a technical corporation with core competitiveness
in the field of interventional and implantation products!
Mission-We are committed to innovation and providing excellent products and service to patient!
By continual innovation, we are committed to providing quality products to satisfy our customers, aiming at sharing advanced medical technology with society.
Barty has passed ISO 13485 quality management system certification approved by TUV-SUD in October, 2016; passed assessment of Chinese medical device registration quality management system in January, 2017; passed ISO 13485 quality management system certification approved by BS in July, 2017.
Barty has established overall process quality management system to make sure that all risks in the product lifecycle are controlled, including design, procurement, production, inspection and improvement, strictly abiding by ISO13485：2003, Appendix to the quality management specification for medical devices: sterile medical devices, Appendix to the quality management specification for medical devices: implantable medical device,MDD93/42/EEC, US.FDA QSR820 and The Pharmaceutical Administration Law of Japan.
Workshop, prodiction, inspection equipment