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About Us

30 years of production experience in China

Liaoning Kangyi Medical Equipment Co., Ltd was founded in 1994 and is one of the leading manufacturers within the health care industry in the Chinese province of Liaoning. Quality is our highest priority, and our quality assurance system is certified and meets the standards of the Chinese National Medical Products Administration, ISO 13485, and the European Union’s CE mark.

We are focused on the production of a wide range of disposable medical finished products and medical components. These include disposable infusion sets, disposable syringes and medical accessories. We produce over 600 million pieces per year. Our products are sold across China and exported worldwide, to destinations including Europe, South America, Russia, Africa, and the Middle East.

Our company employs over 300 staff, including 50 people working in engineering and technical management. Our premises occupy an area of 20,000 square meters, with a construction area of 15,000 square meters. This space includes a 100,000-class purification workshop that occupies 8,000 square meters.

We pride ourselves on maintaining the highest possible standard of customer service. Excellent communication is at the heart of our  approach; our highly professional team is always available to assist our clients. Processing orders efficiently and effectively is our daily work.

We sincerely hope to cooperate with you and invite you to visit our factory. We prioritize the establishment of long and stable relationships with all of our clients, based on our commitment to the highest quality of products and service. We look forward to hearing from you to discuss how Liaoning Kangyi Medical Equipment can best meet your needs.  

Our Factory

20,000 square meters, with a construction area of 15,000 square meters

our Sales

take a closer look

sales person

Emma Chen

Sales Manager

sales person

Wilson Wang

Sales Manager

sales person

Carl Chan

Sales Manager

sales person

Ivy Wu

Sales Manager

Certificate

Comply with REGULATION (EU) 2017/745 on Medical Devices, Annex XI, Part A

ce certificate
CE Certificate MDR 2017/745
iso 13485
ISO 13485

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