Company Profile

BARTY MEDICAL

As a national hi-tech enterprise, Zhejiang Barty Medical Technology Co.,Ltd is committed to the R&D, production and sales of cardio vascular, peripheral vascular and medical equipment with high technology. The products mainly includes paclitaxel eluting PTCA balloon expansion catheter, paclitaxel eluting PTA balloon expansion catheter, paclitaxel-eluting peripheral stent system, PTA balloon catheter, HP PTA balloon catheter, angiography catheter, guide catheter and catheter sheath sets.

With the building area of 5,000 square meters, the company has established the Million level purification (local hundred level) clean workshop in line with the "GMP" requirements, equipped with professional, complete facilities and equipment.

The core management team consists of senior experts and therapists, who have ever worked at international famous foreign medical enterprise for more than 10 years.

Since its foundation, Barty has made many achievements, including about 20 core patents, CE certificate of 5 produces. Fore more, paclitaxel eluting PTCA balloon expansion catheter became the first to get “green channel” approved by SFDA in China. Paclitaxel-eluting peripheral stent system was selected as “2017 Zhejiang Key R&D project.” Barth Medical has already possessed the core competitive products and cutting-edge technologies.

Company Culture

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

Corporate Information