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What material is Y-Type Bond-Tube Luer 3-Way Connector made of?

Quick Answer

The Y-Type Bond-Tube Luer 3-Way Connector (JT-028) is molded from polycarbonate, chosen for the part's connection and fluid-path requirements. The material supports the sterilization and compatibility needs of IV infusion sets and fluid-transfer lines. Custom material and color are available from Baixin Bio.

Definition

A y-type bond-tube luer 3-way connector is one of the small standardized parts that make a medical fluid path work. Its job is to connect, seal or control flow between two segments of a line, and it is manufactured from device-qualified plastics for reliable single-use performance.

Because the part sits directly in the fluid path, three things matter most: a dependable seal, dimensional consistency from part to part, and a material that is compatible with the fluid and the chosen sterilization method.

To put it in context: a disposable fluid-handling device is rarely one molding. It is a chain of small components — connectors, valves, chambers, clamps, caps and tubing — assembled into a single path. Standard interfaces are what let those components come from a catalog and still fit, which is the whole reason this category of part exists.

About This Component

The Y-Type Bond-Tube Luer 3-Way Connector is supplied as a single-use molded part for IV infusion sets and fluid-transfer lines. Its interface follows standard conventions so it mates predictably with compatible components, and it is produced in polycarbonate by default, with other medical-grade resins available on request.

Like all Baixin Bio components, it can be customized for material, color, dimensions, packaging and assembly. For a precise specification — exact dimensions, tolerances, sterilization validation, packaging counts and minimum order quantity — request a drawing and samples through the inquiry form.

Key Advantages

For device assemblers specifying y-type bond-tube luer 3-way connector, the benefits that matter most are reliability and repeatability:

  • Standardized interface that interoperates with compliant luer components
  • Leak-resistant seal that holds under normal line pressure
  • Single-use design that supports sterile, disposable workflows
  • Medical-grade resin selected for fluid compatibility
  • Dimensional consistency across production lots

Taken together, these are the reasons device makers standardize on molded medical components rather than improvising connections: the part is predictable, documented and available at volume, which keeps the finished device safe and the production line moving.

Common Applications

Typical applications for y-type bond-tube luer 3-way connector span the disposable device landscape:

  • Laboratory fluid handling
  • Irrigation sets
  • Disposable diagnostic devices
  • Syringe and pump connections

Across all of these uses, the underlying requirement is the same: a connection that is secure, leak-resistant and safe to make once and discard. That is why standardized, single-use molded components dominate the category — they remove variability from the most failure-prone part of a fluid path, the junction, and they let a device be assembled quickly and qualified as a unit.

How to Specify and Choose

Specifying the right part is mostly about matching a handful of variables to your assembly:

  • The working pressure the junction must hold without leaking or separating
  • The fluid and its chemical compatibility with the candidate resin
  • The inner and outer diameters of the tubing the part bonds to
  • The sterilization method the finished device will undergo
  • Whether the part is single-use or intended for limited reuse

Once these are defined, sample qualification against your own process is the last step before volume. If no catalog part matches, these same inputs drive a custom mold.

Industry Standards

Small-bore connectors for liquids and gases are governed by the ISO 80369 family, which is progressively replacing the historical luer standard to reduce the risk of misconnection between different clinical applications. Medical-grade resins are selected and documented for biocompatibility, and finished components are sterilized by validated methods such as ethylene oxide (EO), gamma irradiation or steam autoclave depending on the material.

For polycarbonate components, the practical sterilization options are gamma and ethylene oxide (EO); the choice is confirmed against the finished device and its validated process.

The reason the standards landscape moved toward ISO 80369 is patient safety: when every line used the same luer taper, it was physically possible to connect, say, an enteral line to an intravenous one. The newer series give different applications deliberately incompatible geometries so a dangerous misconnection cannot be made by accident. For a component maker, that means confirming which series an application requires before specifying a part.

This page is informational and does not replace device-specific regulatory or validation guidance. Confirm exact standards, biocompatibility and sterilization requirements for your product with your quality team and your supplier.

Frequently Asked Questions

Is it compatible with ISO 80369?

Luer interfaces follow small-bore connector conventions. Confirm exact ISO 80369 series compatibility for your application with Baixin Bio before specifying.

What order volumes are supported?

Baixin Bio supplies disposable device assemblers in production volumes, with consistent lot-to-lot quality and export-friendly communication.

Can I request samples?

Yes. Samples and drawings are welcome and recommended before committing to volume. Use the inquiry form to request them.

Is y-type bond-tube luer 3-way connector available for OEM or ODM projects?

Yes. Baixin Bio manufactures to drawings and samples, customizing material, color, dimensions, packaging and assembly. Send your specification for a quote.

What materials are used?

Depending on the part, medical-grade PC, PP, PVC, ABS, PE or POM is used, selected for the connection method, fluid path and sterilization requirement.

How is it sterilized?

Components are compatible with validated single-use sterilization such as ethylene oxide, gamma irradiation or steam autoclave, depending on the resin. Confirm the method for your device.

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Need Medical Connectors or Components?

Baixin Bio manufactures luer connectors, valves, drip chambers, clamps, caps and tubing, with OEM and ODM customization. Send your drawings or samples for a quote.

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