MEDICA 2026 | 16–19 November 2026 | Hall 6, Stall F37 | Düsseldorf, Germany
Explore our flagship, CE and ISO 13485 compliant single-use medical consumables engineered for minimal tissue trauma, zero infection risk, and high volumetric precision.
From raw medical-grade polymer compounding to automated ultrasonic bag seam welding, our integrated production guarantees zero leaks, flawless bio-compatibility, and international regulatory readiness.
All fluid drainage bags, catheter extensions, and vascular access devices are assembled under strictly controlled airborne particulate and bio-burden environments, compliant with ISO 14644-1 standard protocols.
Our urinary and surgical fluid drainage systems incorporate anti-reflux valves (flutter or tower-type) subjected to positive backpressure air and liquid testing to completely eliminate retrograde infection risks.
Equipped with high-precision CNC machinery and injection mold design shops, we tailor bag capacities (500ml to 4000ml), tube lengths, sampling ports, and custom branding without third-party vendor dependencies.
In modern clinical environments—spanning intensive care units (ICUs), post-operative recovery wards, emergency departments, and long-term homecare—the integrity of fluid management systems is directly tied to patient outcomes. As a leading China drainage bag supplier and exporter, our engineering philosophy revolves around preventing Catheter-Associated Urinary Tract Infections (CAUTI), ensuring precise volumetric measurement, maintaining skin integrity, and adhering to strict international biostability criteria.
Fluid drainage bags, bile collectors, leg drainage bags, and urinary meter systems require non-reactive material selection to withstand variable pH levels and prolonged contact with body fluids. We utilize medical-grade virgin PVC compounds, DEHP-free plasticizers (such as TOTM or DINCH), and high-clarity Polypropylene (PP) or Polycarbonate (PC) for rigid chamber components.
Cross-contamination and retrograde bacterial migration represent major hospital-acquired infection (HAI) liabilities. Our closed-system urine drainage bags incorporate engineered safety barrier technologies:
Understanding the exact engineering parameters allows B2B buyers, medical distributors, and tender boards to select optimal SKUs tailored to clinical settings.
| Drainage Bag Category | Standard Capacity | Valve & Drainage Mechanism | Material Specification | Target Clinical Application |
|---|---|---|---|---|
| Standard Closed Urine Bag | 2000 ml / 2500 ml | Anti-Reflux Valve, T-Tap / Push-Pull Valve | Medical PVC (DEHP-Free option), Kink-resistant PVC Tubing | Routine Hospital Inpatient & Post-Surgical Ward Care |
| Precision Urine Meter Bag | 2000 ml Bag + 400 ml Meter | Dual-Chamber Overflow, Needleless Sampling Port, Lever Outlet | Rigid PC Meter Chamber + Flexible Polymeric Bag Body | ICU, Surgical Anesthesia, Critical Renal Function Monitoring |
| Ambulatory Leg Drainage Bag | 500 ml / 750 ml / 1000 ml | Flap Anti-Reflux, Flip-Flo Outlet, Fabric Backing Layer | Textured Non-Woven Backing + Soft Biocompatible PVC | Outpatient, Mobile Rehabilitation & Home Care Patients |
| Pediatric Fluid Collector | 100 ml / 200 ml | Self-Sealing Adhesive Ring, Non-Return Bay | Hypoallergenic Hydrocolloid Adhesive + Micro-Gauge PVC | Infant Urological Sampling & Pediatric Fluid Balance |
| Surgical Wound Drainage System | 400 ml Evacuator / Bag | Negative Pressure Evacuator + Siliconized Drain Catheter | Medical Silicone & High-Resilience Polycarbonate | Orthopedic, Thoracic & General Surgical Fluid Evacuation |
The global medical disposables supply chain is undergoing rapid evolution driven by stringent regulatory frameworks, environmental sustainability mandates, and digitalized supply chain tracking. Procurement officers and importers sourcing from China must align with the following macro trends:
With global healthcare systems focusing on reducing plastic waste, green procurement criteria are gaining traction. Leading manufacturers are introducing thermoplastic elastomers (TPE) and halogen-free compounds that release minimal toxic dioxins upon incineration. Incorporating lightweight yet durable film structures reduces plastic mass per unit without sacrificing tear strength or pressure resistance.
The integration of micro-optical sensors and Bluetooth-enabled smart meters onto closed drainage chambers allows real-time measurement of urinary output, flow rate, and fluid temperature. These automated inputs transmit data directly into Hospital Electronic Health Records (EHR), replacing manual chart logging and flagging acute kidney injury (AKI) indicators early.
With the European Union Medical Device Regulation (EU MDR 2017/745) and US FDA Unique Device Identification (UDI) enforcement, importers must verify that their suppliers provide complete technical documentation, full supply chain traceability, and GMDN/EMDN categorisation. Every unit pack must feature GS1-compliant barcodes to facilitate automated inventory management and clinical safety recalls.
Get authoritative answers regarding minimum order quantities, regulatory dossiers, sterilisation validation, and OEM private-label capabilities.
Every export consignment is backed by a complete regulatory documentation package, including CE Mark Certification (under EU Directive/MDR), ISO 13485:2016 Quality Management System certificates, EC Declaration of Conformity, Certificate of Free Sale (CFS), batch-specific Certificate of Analysis (CoA), and Ethylene Oxide (EO) Sterilisation Validation Reports according to ISO 11135 standards. We also assist with local health authority registrations in South America, Africa, the Middle East, Southeast Asia, and Eastern Europe.
We provide comprehensive OEM/ODM solutions. Importers can customize primary pouch artwork, secondary shelf display boxes, master shipping cartons, multilingual Instructions for Use (IFU), and GTIN/UDI barcode printing. Furthermore, physical design elements—such as tubing length (ranging from 90cm to 150cm), connector types (Luer lock, step connector), sheet thickness, and valve styles—can be customized in our in-house mold tool room.
Our production facilities employ automated high-frequency radio welding and ultrasonic sealing machines that maintain precise temperature, duration, and clamping pressure parameters. 100% of manufactured bags undergo online air-pressure decay testing prior to packaging. In addition, random batch sampling involves burst-pressure hydrostatic testing, seam tensile strength testing, and drop-impact tests according to ISO 8669 standards.
For standard neutral-brand items, the minimum order volume starts at 10,000 units per SKU or 1 mixed FCL container. For custom OEM private-label orders, MOQ is typically 30,000 units depending on printing runs. Production lead time for repeat catalogue orders is 20 to 30 days. First-time OEM programs require 35 to 45 days to complete artwork proofing, film printing, cleanroom assembly, EO sterilisation cycles, and biological indicator quarantine release.
Yes. We offer 100% DEHP-free, phthalate-free, and natural rubber latex-free device configurations across our complete portfolio. Biocompatibility data sheets and ISO 10993 test reports are provided to substantiate safety for sensitive patient groups, pediatric care, and oncology applications.
We routinely quote under FOB, CIF, CFR, EXW, and DDP Incoterms. Ocean freight shipments are loaded directly from major regional hub ports (such as Shanghai, Ningbo, Qingdao, or Nhava Sheva/Mundra depending on plant origin), with air cargo dispatched via international airport terminals. We handle consolidated container loading, palletization, and custom export documentation to ensure seamless customs clearance upon arrival.
Upgrade your supply chain reliability with ISO 13485 certified manufacturing, factory-direct wholesale pricing, and technical support tailored to international medical tenders and distribution channels.
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