Import Endotracheal Tube — Buy in Bulk from Supplier in China

The Endotracheal tube from Zhanjiang Star Medical Co., Ltd. is a single-use medical device designed for airway management during anesthesia, emergency intubation, and mechanical ventilation. It is constructed from medical-grade PVC with a flexible yet durable structure, enabling smooth insertion while minimizing trauma to the tracheal mucosa. The product is available in sizes ranging from 2.0 mm to 10.0 mm internal diameter, catering to neonates, pediatric, and adult patients. Each tube includes an inflatable cuff to prevent aspiration and a radiopaque line running the full length for radiographic verification of placement.

The material complies with ISO 13485 requirements for biocompatibility and does not contain phthalates or latex. The cuff is made from low-pressure, high-volume polyurethane, designed to maintain seal integrity without excessive tracheal wall pressure. Standard tolerances for internal diameter are ±0.2 mm, and wall thickness is consistent across sizes to ensure predictable compliance during ventilation. These characteristics align with EN 13907:2016 and ASTM D3297 standards for endotracheal tubes used in clinical settings.

This product is primarily sourced by hospitals, intensive care units, and emergency medical services in Asia, Africa, and Latin America. Buyers typically order in batches of 500 units or more, packaged in sterile, individually sealed blister packs with a 5-year shelf life. Trade terms include FOB Guangzhou, with lead times of 2 to 4 weeks after deposit. Certifications claimed include CE and ISO 13485, but buyers must request valid copies before shipment. Packaging is non-Ethylene Oxide sterilized unless otherwise confirmed.

Zhanjiang Star Medical Co., Ltd. is registered in Guangzhou, Guangdong, with a physical address listed as 1f Dongfeng East Rd. The company is classified as an imported supplier with harbor trust tier, indicating basic verification of legal registration and physical presence. No details are provided regarding manufacturing capacity, years in operation, or workforce size. The listing does not confirm in-house production or certification audits beyond claimed CE and ISO 13485 status.

The supplier does not publish response rates or average response times, suggesting limited buyer engagement or operational capacity. There is no evidence of clinical testing partnerships, distributor networks, or export history. Buyers should treat this as a trading entity unless verified documentation is provided. No certifications, patents, or quality control protocols are disclosed beyond the product description.