Established in 2005, we are a manufacturer specialized in disposable sterile medical consumables and related single-use devices. We focus on consistent quality, scalable production, and reliable delivery for global OEM/ODM customers.
Our site covers approximately 32,000 m² with a built-up area of over 60,000 m². We operate more than 12,000 m² of ISO Class 8 cleanroom facilities. Sterilization is supported by 8 EO sterilization cabinets. For quality assurance, we run an in-house testing center capable of biological, chemical, and physical testing, with 160+ sets of production equipment and 70+ sets of testing/QC equipment.
Our annual output exceeds 1 billion syringes and 100 million infusion sets. We operate an ISO 13485 certified quality management system and hold EU MDR (EU) 2017/745 QMS certificates (TUV Rheinland) and FDA establishment registrations.