BQ Plus Medical has 700+ employees and serves customers in 50+ countries and regions. The company operates three manufacturing sites and three in-house EO sterilization centers, with approximately 311 m³ total EO chamber capacity per cycle.

BQ Plus Medical operates under an international medical device quality management system, with ISO 13485 certification, FDA registered manufacturing support, FDA 510(k) cleared I.V. Administration Set and I.V. Extension Set products, and documentation support for EU MDR / applicable CE, NMPA, UDI, batch traceability, device history records and complaint handling.

Reliable delivery and quality consistency are core strengths of BQ Plus Medical. The company has maintained 99%+ on-time delivery performance for four consecutive years, supported by integrated production planning, in-house sterilization resources and continuous improvement in manufacturing workflow.