As a professional Chinese Medical Disposable Factory dedicated to the research, development, and manufacturing of single-use medical devices, we supply a comprehensive range of nursing care products to hospitals, clinics, and healthcare procurement teams worldwide. Our Nursing Care Category covers critical bedside tools used in respiratory nursing, intravenous infusion management, neonatal care, and postpartum recovery. Every product in this line is manufactured under strict quality control standards, compliant with ISO 9001, CE, and NMPA GMP requirements, and engineered to reduce cross-contamination risk while improving procedural efficiency for clinical staff.
Founded in 1992 and headquartered in Jiaxing, Zhejiang Province, China, our factory operates over 110,000 m² of Class 100,000 clean room space, employs more than 180 professional technicians, and holds over 80 registered patents. With annual export coverage across 30+ countries and regions, we have established long-term supply partnerships with hospitals and distributors across Europe, North America, Southeast Asia, and the Middle East. Learn more on the About Us page or visit our R&D center overview to understand our continuous innovation philosophy.
Our Disposable Respiratory Suction Catheter is a single-use, sterile tube designed for the safe aspiration of phlegm, mucus, and secretions from the oral cavity, nasal passage, or trachea. It is widely applied in ICU settings, post-operative recovery rooms, and general wards where patients are unable to independently clear their airways due to unconsciousness, intubation, or respiratory compromise.
The catheter is manufactured from medical-grade PVC (polyvinyl chloride) or soft-segment thermoplastic elastomer, selected for its flexibility, smooth inner wall surface, and low friction coefficient. The tube's rounded tip design minimizes mucosal trauma during insertion, while the transparent body allows real-time visual monitoring of secretion volume and color — a critical clinical indicator for assessing infection status or bleeding. Multiple lateral holes near the distal end improve suction coverage and prevent tip occlusion.
Available in French sizes ranging from Fr6 to Fr18 (approximately 2.0 mm to 6.0 mm outer diameter), the tube accommodates both pediatric and adult patients across nasal, oral, and tracheal suction procedures. Each unit is individually packaged in a peel-open sterile pouch and is EO (ethylene oxide) sterilized. Shelf life is typically five years from the date of manufacture under recommended storage conditions (temperature below 25°C, away from direct sunlight and moisture).
From a technical compliance perspective, the product is manufactured in conformance with ISO 10555 (intravascular catheters) as a reference standard and the relevant national standards for single-use suction catheters (YY/T 0341 in China). Our quality system is certified under ISO 13485:2016, and our export versions carry CE marking (MDD/MDR Class IIa). Hospitals sourcing this product benefit from sterile, single-use design that eliminates the need for reprocessing infrastructure while reducing HAI (healthcare-associated infection) transmission risk.
For facilities requiring closed-circuit suctioning — particularly for mechanically ventilated patients — we also supply the Disposable Closed Suction Catheter, which maintains ventilator circuit integrity during suction procedures, reduces aerosol exposure, and is recommended by infection control guidelines for COVID-19 and other airborne-risk patients.
Our Infusion and Transfusion Pressure Bag is a pneumatically operated external compression device designed to accelerate the delivery rate of intravenous fluids, blood products, or contrast media beyond the flow rate achievable by gravity drip alone. It is an essential tool in trauma resuscitation, rapid volume replacement, surgery, and emergency medicine.
The pressure bag consists of an outer shell made from medical-grade Oxford nylon or polyester fabric, an inner air bladder constructed from thermoplastic polyurethane (TPU) film, a calibrated pressure gauge (manometer), a hand bulb pump with one-way valve, and a quick-release pressure valve. The outer pouch accommodates standard 500 mL and 1000 mL infusion bags or blood bags, secured via hook-and-loop (Velcro) closure strips or zipper design depending on model variant. The inner air bladder uniformly distributes compression force across the entire surface of the IV bag, avoiding localized pressure points that could rupture the bag or cause uneven flow.
The integrated pressure gauge is clearly graduated in mmHg (0–300 mmHg), allowing clinical staff to precisely maintain the target pressure — typically 200–300 mmHg for rapid resuscitation, per standard clinical protocols. The hand bulb pump allows rapid inflation, while the quick-release valve enables immediate decompression and bag exchange. Transparent windows on the outer shell allow the IV bag fill level to be monitored without removing the device.
From a material safety standpoint, all components in contact with the IV bag surface are free from DEHP (di(2-ethylhexyl) phthalate) and latex, eliminating sensitization risk and ensuring compatibility with all standard infusion bag films. The product is reusable and designed for repeated autoclave sterilization (121°C, 15 min) or disinfection with alcohol-based agents according to hospital protocols. Units are supplied in cleanroom-packed sterile or non-sterile configurations depending on procurement requirements.
Our pressure infusion bag product line is complementary to the broader Infusion Category solutions we offer, which include standard and precision infusion sets, extension tubes, three-way stopcocks, and IV filters — enabling procurement teams to source a complete infusion management system from a single validated manufacturer.
Our Disposable Umbilical Cord Clamp is a single-use locking clamp used to ligate and occlude the umbilical cord immediately after delivery, preventing neonatal blood loss and minimizing risk of omphalitis (umbilical stump infection). It is among the most widely used and standardized neonatal care consumables in obstetric departments, delivery rooms, and midwifery settings worldwide.
The clamp body is injection-molded from medical-grade ABS (acrylonitrile butadiene styrene) resin or polypropylene, chosen for its rigidity, chemical stability, and biocompatibility. The clamping mechanism uses a ratchet-lock design that closes in a single action and locks irreversibly, preventing accidental release after application. The serrated inner jaw surfaces provide a secure grip on the cord tissue, maintaining occlusion under normal neonatal movement and handling conditions. The clamp profile is flat and low-profile to minimize discomfort to the neonate and simplify diaper placement in the days following delivery.
Typical physical specifications include a clamp width of approximately 12–14 mm and a jaw opening clearance suitable for cord diameters from 8 mm to 14 mm, covering standard to hypertrophic cord presentations. Each unit is individually packaged in a peelable sterile blister and EO sterilized. A color-coded identification system (available in white, yellow, or blue by request) helps delivery room staff distinguish maternal versus neonatal supplies and batch-track usage in busy obstetric units.
Regulatory compliance for this product includes ISO 10993 biocompatibility testing series (cytotoxicity, sensitization, intracutaneous reactivity), ISO 11135 (EO sterilization validation), and registration under NMPA Class II medical device approval. CE-marked versions are available for European hospital procurement. Our factory was among the first batch of Chinese medical device manufacturers to pass the NMPA GMP pilot acceptance program (2007), making our quality infrastructure one of the most rigorously audited in the sector.
For comprehensive neonatal and postpartum nursing supply, this product is frequently co-sourced alongside our Postpartum Blood Collector, which is used to measure and collect postpartum hemorrhage volume for clinical assessment and record-keeping — a product that completes our neonatal and maternal care consumables portfolio.
Our Nursing Care Category is one of seven major clinical product series manufactured at our Jiaxing factory. The full nursing care range currently includes the Disposable Respiratory Suction Catheter, Disposable Closed Suction Catheter, Infusion and Transfusion Pressure Bag, Disposable Umbilical Cord Clamp, and Postpartum Blood Collector. Each product is available in multiple configurations and packaging specifications to meet the purchasing requirements of government hospital tenders, private healthcare groups, and international distributors.
For facilities procuring across multiple clinical departments, our product portfolio extends into General Anesthesia consumables, Regional Anesthesia kits, Monitoring Category accessories, Pain Management devices, and Medical Aesthetics disposables — enabling consolidated supply chain management with a single ISO-certified manufacturer. Our factory maintains a dual-track quality system for both domestic NMPA-registered products and export-certified products (CE/FDA), giving international buyers confidence in regulatory traceability.
All products are manufactured under Class 100,000 cleanroom conditions in accordance with ISO 14644-1 standards for particulate contamination control. Batch traceability records are maintained for a minimum of ten years post-manufacture in compliance with MDR (EU) 2017/745 and Chinese national device tracking regulations.
Sourcing from a vertically integrated Chinese Medical Disposable Factory with decades of production experience provides several procurement advantages over trading company intermediaries. Direct factory pricing reduces landed cost by eliminating middlemen markups. In-house R&D capabilities — supported by our Macromolecule Medical Device Joint R&D Laboratory established in collaboration with Zhejiang University — mean we can accommodate OEM customization, private labeling, and product modification requests with shorter lead times. Our factory's patent portfolio of 80+ registered innovations reflects ongoing technical advancement rather than static product lines.
Quality assurance is backed by multi-stage inspection protocols including incoming raw material verification, in-process statistical sampling (AQL 2.5 standard), finished product 100% leak testing where applicable, and final sterility assurance level (SAL) of 10⁻⁶ for all EO-sterilized items. Factory audit support is available for procurement teams and regulatory consultants requiring on-site qualification visits.
To request product specifications, sterility certificates, regulatory documentation, or a commercial quotation, visit our Contact page or reach us directly at global@zjsj.com.cn. Our export team based in Jiaxing, Zhejiang responds to international inquiries within one business day.
