Jiangsu Ruitian Medical Technology

Jiangsu Ruitian Medical Technology Co., Ltd. was established in 2018, mainly engaged in the research and development, manufacturing and sales of endoscopic minimally invasive medical devices. The company introduces advanced foreign technology, works closely with well-known universities and scientific research institutions, continuously optimizes product structure, stabilizes product quality, and meets customer needs. The company is located in Hutang Science and Technology Industrial Park, Wujin, Changzhou. It has an existing purification workshop of 20,000 square meters and an annual output of one million biopsy forceps.

The Engineering Technology Center currently has 10 full-time R&D personnel, including: 1 doctor, 5 undergraduates, 4 college students; 1 senior professional title, 5 intermediate professional titles, and 10 junior professional titles.

The company focuses on industry-university-research cooperation. Now Changzhou University, Jiangsu Institute of Technology and many other scientific research institutions and universities have established scientific research and production consortiums; in order to enhance the key links of the company’s technological innovation capabilities, the company has also established a research and development center in Zhejiang to a larger scale Integrate resources, expand advantages, and improve market competitiveness.

On the basis of ordinary disposable live sampling forceps, we have developed an exclusive and innovative disposable rotary live sampling forceps, which can rotate 360 degrees accurately and synchronously; it solves the dead spots in different angles of sampling during the operation, thereby greatly improving Doctor’s and surgical efficiency. At the same time, the disposable foreign body forceps, disposable electric snares, and disposable hot biopsy forceps launched on this basis all have a synchronous rotation function.

The company has established a complete quality system in accordance with ISO13485, "Medical Device Manufacturing Quality Management Regulations" and EU regulations. The company has passed the ISO13485 quality system certification of TUV South Germany and the EU CE product certification.

The company has passed the on-site inspection of the product certification of the domestic drug regulatory system, and has obtained 7 domestic product registration certificates, namely, single-use rotary live sampling forceps, single-use live sampling forceps, and single-use cervical live sampling forceps. One-time use of foreign body forceps, one-time use of cell brushes, one-time use of endoscopic injection tubes, and one-time use of bile duct drainage tubes.