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Female luer connector

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Commonly Used:
US$
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Customization Available
Sample Available
Manufacturer First
Product Attributes:
Surgical Supplies Materials
Type: Face Mask/Apron/Gloves
Type: Infusion Set
Material: Plastic
Ethylene Oxide Sterilization
Quality Guarantee Period: Two Years
Group: Adult
With Logo Printing
Surface Treatment: Without Treatment
Head Type: Round
Precision: Precision
Condition: New
Certification: RoHS
Warranty: 6 Months
Automatic Grade: Manual
Processing Object: Metal
Molding Style: Forging
Application: Hardware
Heat Treatment: Quenching
Forging Tolerance: +/-0.5mm
Material: SS
Without Ethylene Oxide Sterilization
Without Logo Printing
Surface Treatment: Passivation
Certification: ISO
Certification: ISO 9001:2000

Sourcing guidance for Female Luer Connector

What are the critical technical standards for Female Luer Connectors in medical applications?

The most vital standard is ISO 80369-7 (which replaced ISO 594), ensuring dimensional compatibility and leak-proof performance for intravascular or hypodermic applications. Buyers must verify that the connectors are BPA-free, non-toxic, and medical-grade, typically using materials like Polypropylene (PP), Polycarbonate (PC), or Nylon. For sterile environments, ensure the material is compatible with Ethylene Oxide (EO) or Gamma radiation sterilization.

How do I choose between a Luer Lock and a Luer Slip female connector?

The choice depends on the pressure requirements of the application. A Luer Lock female connector features threads that securely screw onto a male housing, preventing accidental disconnection in high-pressure fluid delivery. A Luer Slip relies on friction fit and is suitable for low-pressure, quick-connection scenarios. For critical medical or laboratory fluid paths, Luer Lock is the industry standard for safety.

What material properties should be prioritized for chemical resistance?

If the connector will be exposed to aggressive chemicals or solvents, Polyvinylidene Fluoride (PVDF) or Polytetrafluoroethylene (PTFE) should be selected for their superior chemical inertness. For standard saline or lipid infusions, Polycarbonate is preferred for its transparency and high impact resistance, allowing for easy visual inspection of air bubbles or fluid flow.

What are the key quality control benchmarks for bulk procurement?

Suppliers should provide evidence of 100% leak testing and dimensional accuracy checks using calibrated plug gauges. Look for a Class 100,000 cleanroom production environment to minimize particulate contamination. Requesting a Certificate of Analysis (CoA) for every batch is essential to ensure consistency in tensile strength and thread integrity.

Cross-Border Procurement Strategy for Luer Components

How can I mitigate quality risks when sourcing from overseas suppliers?

Always request pre-shipment samples and verify the supplier's ISO 13485 certification, which is specific to medical device quality management. Utilize Made-in-China.com's Secured Trading services to ensure payment is only released after the goods pass a third-party inspection (such as SGS or Intertek) at the factory.

What are the common pitfalls in international shipping for small medical components?

Due to their small size and high precision, Female Luer Connectors are prone to crushing or contamination if poorly packaged. Insist on double-layered vacuum packaging or anti-static bags inside rigid outer cartons. For shipping to the US or EU, ensure the HS Code (typically 3917.40) is correctly declared to avoid customs delays or incorrect tariff applications.

How should I negotiate pricing and lead times for high-volume orders?

For orders exceeding 50,000 units, aim for a tiered pricing structure where the unit cost drops by 15-25%. Negotiate a rolling forecast agreement where the supplier maintains a safety stock of 10% to reduce lead times from the standard 20-30 days down to 7 days for repeat orders.

What regulatory documentation is required for importing medical connectors?

Ensure the supplier provides a Declaration of Conformity (DoC) and, if applicable, FDA 510(k) clearance or CE marking. For non-medical industrial use, a REACH and RoHS compliance certificate is usually sufficient to clear customs in most developed markets.

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