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Urine bag connector

I have found results from3000+products and1000+suppliers aboutUrine bag connector

Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Type: Drainage Container/Tube
Type: Infusion Set
Type: Catheter
Material: Plastic
Ethylene Oxide Sterilization
Group: Adult
Quality Guarantee Period: Two Years
With Logo Printing
Feature: Disposable
Certification: CE
Application: Hospital
Shaping Mode: Injection Mould
Surface Finish Process: Polishing
Mould Cavity: Multi Cavity
Plastic Material: ABS
Runner: Cold Runner
Design Software: UG
Installation: Mobile
Standard: HASCO
Customized: Customized
Kind: Thermoplastics Pipes
Water Absorption: 0.2%~0.3%
Contraction Percentage: 0.4%~1.4%
Tensile Strength: 30~40MPa
Character: Environmental Protection
Species: Housing
Production Process: Injection Molding
Shape: Round
Interface Type: DC/DC
Driven Type: Electric
Condition: New
Warranty: 12 Months
Automatic Grade: Semiautomatic
Material: PP
Without Ethylene Oxide Sterilization
Without Logo Printing
Feature: Reusable
Certification: ISO13485
Certification: TS16949
Certification: ISO
Certification: BS
Certification: UL
Certification: VDE
Application: Car
Application: Household Appliances
Application: Furniture
Application: Commodity
Application: Electronic
Application: Home Use
Application: Hardware
Contraction Percentage: 1.0%~2.5%

Sourcing guidance for Urine Bag Connector

What are the key material requirements for medical-grade urine bag connectors?

Connectors must be manufactured from medical-grade PVC, PP (Polypropylene), or PE (Polyethylene) that is BPA-free and DEHP-free to ensure patient safety. The material must be biocompatible according to ISO 10993 standards to prevent allergic reactions or toxicity during prolonged skin or fluid contact.

Which international compliance standards should a B2B buyer verify?

Suppliers must provide CE Marking (EU) and FDA Registration (US) for Class I or Class II medical devices. Additionally, the manufacturing facility should hold ISO 13485 certification, which specifically governs quality management systems for medical devices. Ensure the product meets EN 1616 standards for sterile drainage catheters and accessories.

What technical features ensure a leak-proof and secure connection?

Look for connectors with a universal stepped design (Christmas tree adapter) to ensure compatibility with various catheter sizes. A secure locking mechanism (Luer lock or friction fit) is essential to prevent accidental disconnection. The surface should be smooth and burr-free to maintain a closed system and reduce the risk of Catheter-Associated Urinary Tract Infections (CAUTI).

How should sterilization and packaging be evaluated for bulk imports?

Products must be EO (Ethylene Oxide) sterilized or Gamma irradiated. Each unit should be housed in a medical-grade blister pack or peel-pouch with a clear sterility indicator. The packaging must display the expiry date, lot number, and sterilization method to ensure full traceability in clinical environments.

Cross-Border Procurement & Risk Management for Medical Consumables

How can I mitigate quality risks when sourcing medical connectors from overseas?

Request a Pre-Shipment Inspection (PSI) by a third-party agency like SGS or Intertek to verify that the dimensions, seal integrity, and tensile strength match the approved samples. Always use Made-in-China.com’s Secured Trading services to ensure payment is only released after the goods pass quality verification.

What are the best strategies for negotiating with medical plastic manufacturers?

Focus on long-term volume commitments rather than one-off orders to secure lower unit prices. Negotiate for free replacement of defective units (aim for a defect rate of <0.5%) and request customized labeling (OEM) to include your brand and local regulatory information at no extra cost for high-volume orders.

What shipping precautions are necessary for sterile medical components?

Ensure the outer cartons are double-walled corrugated fiberboard to prevent crushing. The shipping environment must be cool and dry; avoid high-humidity containers which can compromise the integrity of the sterile paper pouches. Specify 'Medical Supplies - Handle with Care' labeling on all pallets.

How do I ensure compliance with international trade policies for medical devices?

Verify the HS Code (typically 9018.90) to determine applicable import duties and VAT in your country. Ensure the supplier provides a Certificate of Free Sale (CFS) and a Declaration of Conformity, which are often required by customs to clear medical-grade plastic components.

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