OVERVIEW For Paclitaxel Coated-PTCA Balloon Catheter
The specifically designed and exclusively CFDA approved high pressure DCB for the treatment of shunt stenosis.
FLOWTY DCB protects AV fistulas and shunt grafts from early restenosis.
For the prevention and successful dilatation of intimal hyperplasia.
INDICATIONS for Paclitaxel Coated-PTCA Balloon Catheter
FLOWTY DCB is suitable for new generation, restenosis or stent restenosis of superficial femoral artery or popliteal artery, and the reference vessel diameter is 4-7mm.A drug on a balloon is released into the blood vessel to treat a narrow lesion.

PRODUCT DETAILS FOR Paclitaxel Coated-PTCA Balloon Catheter
Shunt restenosis represents a common threat to the function of arteriovenous fistulas (AVFs) and shunt grafts in patients on hemodialysis. Patients often develop a consecutive neointimal hyperplasia in hemodialysis access vessels as well as along the needle puncture site.
The new APERTO DCB Paclitaxel releasing, high pressure balloon dilatation catheter provides a dual shunt treatment quality for the prevention and dilatation of intimal hyperplasia. AVF or PTFE shunt graft venous outflow lesions can be treated very successfully by the new APERTO OTW leading to a substantial reduction of hemodialysis shunt restenosis, for a prolonged dialysis access survival
Paclitaxel Coated-PTCA Balloon Catheter PRODUCT FEATUURES
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Nano-needle crystals-drug coating is more efficient, Without excipients, ensuring the purity of paclitaxel,
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Drug coating is more uniform, more stable ,Conducive to high transfer rate of blood vessel.
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Nano-needle crystals-long term maintenance of effective drug concentration
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Semi-compliant balloon
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Very small passing diameter
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Excellent passability
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Excellent push performance
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Outer diameter lower than the competition

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
Company Culture
Vision & Goal - Barty is committed to becoming a technical corporation with core competitiveness
in the field of interventional and implantation products!
Values-
Gratefulness
Co-creating
Win-win
Sharing
Mission-We are committed to innovation and providing excellent products and service to patient!
Quality System
01.Quality Principle
By continual innovation, we are committed to providing quality products to satisfy our customers, aiming at sharing advanced medical technology with society.
02.System Certification
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.
03.Quality Guarantee
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.
04.Hardware Advantages
Workshop, prodiction, inspection equipment
CONTACT WAY
Name: Amanda Zhu
Email: qqzhu@batymedical.com
Mobile: +86 157 0559 1759 (whatsapp)
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