Nordi Medical
Nordi Medical
Explore our CE & ISO certified healthcare configurations built for hospitals, clinical institutions, and wholesale global procurement networks.
Ensuring optimal anatomical delivery, material stability, and compliance with the medical system regulations.
Enteral tubes designed and exported under strict adherence to EU MDR 2017/745 regulations. Our products undergo rigorous clinical evaluation, biological compatibility assessments, and manufacturing stability tests to ensure optimal reliability.
Integrating standard connectors to eliminate misconnection hazards with intravenous or neuraxial lines. Our engineering department ensures structural compliance, minimizing adverse patient outcomes in complex critical care pathways.
We prioritize Medical-Grade Polyurethane (PUR) and premium Silicone formulations. Our feeding tubes offer optimal structural strength, resist gastric acid degradation, and soften inside the gastrointestinal tract to match patient temperature.
Sourcing enteral feeding devices from a leading manufacturer in China provides substantial technological and logistics advantages. Over the past decades, production hubs in regions like Zhejiang have integrated advanced raw material synthesis with automated extrusion technologies. This enables the production of high-precision nasogastric (NG), nasojejunal (NJ), and gastrostomy tubes at a fraction of Western production costs without compromising clinical efficacy.
At our state-of-the-art facilities, we employ class 100,000 cleanrooms and automatic visual inspection systems to test tube wall thickness, flow path uniformity, and structural integrity. Every millimeter of our medical-grade polyurethane feeding tubes features a co-extruded radiopaque line, ensuring precise positioning under X-ray verification. This rigorous control of tolerances, coupled with high-speed EO (Ethylene Oxide) sterilization tunnels, ensures that massive volume orders are fulfilled safely, uniformly, and efficiently.
From ICU clinical support to home enteral nutrition (HEN), our tubes adapt to specific patient demographics and delivery methods.
In high-acuity wards, patients frequently require long-term nutritional support. Our feeding tubes with weighted tips allow for rapid post-pyloric placement, minimizing gastric retention and lowering the risk of ventilator-associated pneumonia (VAP).
For neonates and pediatric patients with developing systems, comfort and bio-compatibility are essential. We manufacture micro-bore feeding tubes (from 3.5 Fr to 6 Fr) that are soft, highly flexible, and free of DEHP/phthalates.
Established in 1992, Hangzhou Nordi Medical Co., Ltd. is a leading manufacturer and exporter specializing in the production of high-quality medical dressings and related healthcare products. With a registered capital of 5.8 million yuan, we have grown to become a prominent player in the medical industry, providing a wide range of innovative solutions to global markets.
At Nordi, we are committed to upholding the principle of “Quality First, Customer First” in every aspect of our operations. Our products are renowned for their outstanding quality, which has earned us a solid reputation and trust from our clients worldwide. This commitment to quality forms the foundation for our sustainable growth and continued development in the global market. Our products are widely distributed across major markets, including North America, Europe, Southeast Asia, and beyond.
Since our establishment, we have continuously advanced our technology by incorporating both domestic and international innovations. We actively invest in training and development for our technical staff to ensure that our teams are equipped with the expertise needed to drive innovation and excellence. Our business philosophy is centered around continuous improvement and operational efficiency. We have established a robust management system that guarantees high standards in all aspects of production and customer service.
Nordi Medical places a significant emphasis on technological advancements and the continuous upgrading of our production equipment. By focusing on the finer details of the manufacturing process, we have achieved breakthroughs in product development, ensuring that we remain at the forefront of the medical supply industry. With a clear vision for the future, we are building a strong, sustainable business model that aligns with industry standards and market demand.
Over the years, we have expanded from a small workshop with an annual output value of just 2 million yuan and an area of 1,000 square meters into a large-scale, standardized production and marketing enterprise. Today, we operate a modern facility that is capable of meeting the demands of a global market, ensuring high-quality products and fast delivery times.
Our unwavering belief in "Quality First, Customer First" guides our every decision and action. This principle is deeply ingrained in the fabric of our company and has been key to our long-term success.
Quality control is at the heart of everything we do. We adhere to strict quality management systems to ensure that our products meet the highest international standards. This commitment to quality is essential to our continued success and growth.
Innovation drives our future. At Hangzhou Nordi Medical, we embrace change and strive to lead in the development of new products and technologies. We are dedicated to staying ahead of industry trends and continually evolving to meet the diverse needs of our customers.
Providing global healthcare buyers, distributors, and group purchasing organizations (GPOs) with structured sourcing solutions.
We offer extensive customization for sizing (from 3.5 Fr to 18 Fr), length, printing styles, radiopaque stripes, and color-coded ENfit connectors to align with your regional clinical guidelines.
From checking the raw polyurethane resins to inspecting the finished sterilized products, every batch is recorded in our ERP system. This ensures complete traceability under ISO 13485 requirements.
Our location in Hangzhou offers convenient access to Ningbo and Shanghai ports. We leverage this strategic position to coordinate efficient sea, air, and multimodal logistics, reducing lead times.
Answers to common clinical, quality assurance, and technical questions regarding our feeding tube systems.
Polyurethane (PUR) offers superior biocompatibility and durability compared to PVC. While PVC tubes contain plasticizers like DEHP which can leach out and cause the tube to stiffen over time, PUR is inherently elastic and does not require plasticizers. Additionally, PUR tubes soften inside the gastrointestinal tract in response to body temperature, reducing mucosal irritation and patient discomfort. The material's strength also allows for thinner tube walls and a larger internal diameter, which helps improve flow rates and reduce the risk of clogging.
We supply enteral feeding tubes configured with ENfit® connectors compliant with ISO 80369-3 standards. These connectors feature a unique design that is incompatible with Luer lock fittings or other connectors used for intravenous or neuraxial delivery. This physical incompatibility helps prevent accidental misconnections, ensuring patient safety in busy hospital environments.
All our sterile medical supplies, including feeding tubes and surgical drapes, undergo EO (Ethylene Oxide) sterilization validated under ISO 11135 standards. We monitor every sterilization batch using chemical indicators and biological indicators. Products are held in aeration chambers until EO residual levels fall well below the limits specified in ISO 10993-7, ensuring safe application in clinical settings.
Yes. As an OEM manufacturer, we can customize enteral feeding systems to meet specific market demands. We can modify tube lengths, print custom centimeter indicators, adjust the placement of radiopaque lines, and change the tip design (e.g., weighted vs. unweighted tips, open vs. closed distal ends) to suit various clinical needs.
Our regulatory team maintains comprehensive technical documentation, including risk management files (ISO 14971), clinical evaluation reports (CER), and strict post-market surveillance (PMS) procedures. This ongoing compliance ensures that our CE certificates remain valid under the latest European medical device standards.
Additional medical consumables, polymers, and chemical products manufactured to rigorous quality standards.
