Manufacturing Facilities

Automation, precision, and strict quality control - this is how we manufacture medical consumables for global healthcare markets.

Our modern cleanroom production facility features advanced automated equipment designed to ensure stable quality, high production efficiency, and reliable product performance.

From disposable blood collection tubes to infusion products, we are committed to delivering dependable medical consumables trusted by global partners.

Every EDTA Tube undergoes rigorous quality inspections throughout the manufacturing process-from raw materials to final packaging-to ensure compliance with international quality standards.

Regulatory Support

Documents

We provide comprehensive regulatory support for blood‑collection‑tube partners, including certificate provision and registration assistance to accelerate global market access.

Available certificates and export documents (product‑applicable): ISO 13485 QMS certificate, CE certificate, FSC (Free Sale Certificate), manufacturer's Declaration of Conformity, batch‑wise COA, manufacturing license, biocompatibility test reports and sterilization validation. We also supply commercial export documents for customs clearance and tender use.

Registration

We assist customers for local registration. Our team reviews OEM label and packaging drafts to check symbols, mandatory markings and warning statements against international standards. We provide document checklists and technical data required for target‑market submission.

Please note we do not serve as local authorized representative, local registration procedures shall be completed by customers' local agent. Full batch records are well‑maintained to support post‑market surveillance, authority audits and complaint handling.