Import Central Venous Catheter — Buy in Bulk from Supplier in China

The central venous catheter from PLS Minimally Invasive Interventional Medical Co., Ltd. is a medical-grade device engineered for vascular access in critical care environments. It features a smooth, tapered tip for atraumatic insertion, and is constructed from biocompatible medical polymer to minimise infection risk. The catheter is supplied sterile, with individual packaging suitable for immediate clinical use.

Available in multiple French sizes to accommodate diverse patient anatomies and procedural requirements, this catheter is compatible with standard infusion and blood sampling protocols. Typical industry variants include single-lumen, double-lumen, and triple-lumen configurations, with standard lengths ranging from 15 cm to 30 cm. Material composition is commonly polyurethane or silicone, both of which offer flexibility and durability for prolonged dwell times.

Hospitals and oncology centres use this device for administering chemotherapy, parenteral nutrition, and frequent blood draws. Critical care units rely on it for rapid fluid resuscitation and central venous pressure monitoring. Buyers should confirm lumen count, size, and tip design with the supplier, as these parameters directly impact clinical application. The product is intended for single-use to prevent cross-contamination.

PLS Minimally Invasive Interventional Medical Co., Ltd. is based in Zhongshan, Guangdong, China, with its operations centred in the National Health Industry Park. The company specialises in minimally invasive medical devices, including vascular access products. Its address at Pls Building, No. 6, Jingyue Road, places it within a dedicated health industry zone, indicating a focus on medical manufacturing.

The supplier is classified under the imported tier with a harbor trust tier, though its current response rate and average response hours are not available. The company’s profile does not specify certifications, production capacity, or client base, so buyers should directly verify compliance with ISO and CE standards, as well as other regulatory requirements for their target markets. No additional details on company history, workforce, or revenue are provided in the listing.