INDUSTRY COMPONENT

Luer Lock Connector

A standardized medical connector for secure, leak-proof fluid transfer in syringes and medical devices.

Component Specifications

Definition
A Luer Lock Connector is a standardized medical-grade component designed to provide a secure, leak-proof connection between syringes, needles, catheters, and other medical devices. It features a threaded locking mechanism that prevents accidental disconnection during fluid transfer, ensuring safety and reliability in medical applications. The connector conforms to ISO 80369 standards for small-bore connectors to prevent misconnections.
Working Principle
The Luer Lock operates on a screw-thread locking principle. The male connector (typically on the syringe) has external threads, while the female connector has internal threads. When connected, the threads engage and are tightened to create a secure mechanical lock. This prevents accidental disconnection due to pressure or movement, while maintaining a fluid-tight seal through the tapered Luer slip interface.
Materials
Medical-grade polypropylene (PP), complying with USP Class VI, ISO 10993 biocompatibility standards. May include additives for color coding, radiopacity, or enhanced chemical resistance.
Technical Parameters
ParameterTypical rangeNotes & selection driver
Taper6% Luer taper (ISO 594-1)
LeakageZero leakage at rated pressure
Thread Size6% Luer Lock thread (ISO 594-2)
SterilizationAutoclavable (121°C, 15 psi), Gamma radiation, EtO compatible
Pressure RatingUp to 400 kPa (58 psi)

Ranges are indicative industry figures for RFQ preparation, not a supplier commitment. Confirm every value and standard with the legal manufacturer before ordering.

Standards
ISO 80369-7, ISO 594-1, ISO 594-2, USP <381>, ANSI/HIMA MD70.1

Parent Products

This component is used in the following industrial products

Engineering Analysis

Risks & Mitigation
  • Cross-contamination if not properly sterilized
  • Thread stripping from overtightening
  • Misconnection with non-Luer devices (mitigated by ISO 80369)
FMEA Triads
Trigger: Incorrect thread engagement during assembly
Failure: Leakage or disconnection during fluid transfer
Mitigation: Implement visual/tactile alignment guides and torque-controlled assembly processes
Trigger: Material degradation from repeated sterilization
Failure: Cracking or thread deformation
Mitigation: Use medical-grade polypropylene with sterilization cycle validation and replacement protocols

Industrial Ecosystem

Compatible With

Typical Suppliers & Equivalents

Compliance & Inspection

Tolerance
±0.1 mm on critical dimensions per ISO 80369-7
Test Method
Pressure decay test per ISO 80369-7, extractables testing per USP <661.1>, biocompatibility per ISO 10993

Procurement Evaluation Criteria

A practical evidence checklist for RFQ preparation and supplier evaluation.

Technical documentation
Request current drawings, revision history, and a signed specification sheet.
Manufacturing capability
Verify equipment lists, process limits, capacity, and representative production evidence.
Inspection readiness
Confirm test methods, calibrated equipment, sampling plans, and traceable reports.
Supplier transparency
Check the legal entity, factory address, ownership, certifications, and direct contacts.

CNFX does not score or rank suppliers. Buyers must verify all claims and documents with the legal manufacturer before ordering.

Manufacturers of Luer Lock Connector

Manufacturer profiles associated with Luer Lock Connector.

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Frequently Asked Questions

What is the difference between Luer Lock and Luer Slip connectors?

Luer Lock connectors have a threaded locking mechanism for secure connections, while Luer Slip connectors rely on friction fit without threads. Luer Lock is preferred for high-pressure or critical applications to prevent accidental disconnection.

Are Luer Lock connectors standardized globally?

Yes, Luer Lock connectors follow ISO 80369-7 standards to ensure global compatibility and prevent misconnections with other medical device connectors.

Data Basis

Editorial classification, named public sources where available, and source-reviewed manufacturer records. See the editorial policy.

Preliminary Technical Classification
This page supports structured research, RFQ preparation, and supplier evaluation. It does not replace buyer-led supplier qualification, standards review, or technical approval.

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