The Enteral Feeding Flush End Connector (JT-050) suits IV infusion sets and fluid-transfer lines and similar single-use fluid-handling assemblies. It is molded from medical PVC for dependable connections. ' . bfaq_company_name() . ' offers it as a standard or customized part.
Definition
An enteral feeding flush end 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.
What separates a medical-grade part from a generic fitting is repeatability. Sealing surfaces are smooth and consistent, dimensions hold across the lot, and the resin is selected for fluid compatibility and sterilization.
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 Enteral Feeding Flush End 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 medical PVC 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
The reasons enteral feeding flush end connector is specified come down to a few concrete advantages:
- 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
In short, the component earns its place by being unremarkable in the best way: it fits, it seals, it is available, and it behaves the same every time, so engineering attention can go to the device rather than the fitting.
Common Applications
In practice, enteral feeding flush end connector appears wherever a controlled fluid connection is needed:
- Disposable diagnostic devices
- Syringe and pump connections
- IV infusion sets
- Blood and fluid transfer lines
What links these applications is risk. Each one moves fluid into or out of a patient or a sample, so a leak, a wrong connection or a contaminated surface has consequences. Standardized single-use components reduce that risk by making every junction predictable and by being discarded rather than reprocessed, which is the safer default for most modern disposable devices.
How to Specify and Choose
A good specification answers a short list of questions up front:
- 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
- Color coding or opacity requirements for the assembly
- Packaging format and order volume for the program
With those answers in hand, a supplier can confirm a standard part or scope a custom one without back-and-forth. Sharing a drawing or a physical sample removes the remaining ambiguity.
Industry Standards
Two standards questions dominate this category: connection geometry and sterilization. Connection geometry is increasingly defined by the ISO 80369 series, which separates applications so incompatible lines cannot mate; sterilization is handled by validated EO, gamma or steam autoclave processes matched to the resin and the device.
For medical PVC components, the practical sterilization options are EO and gamma; the choice is confirmed against the finished device and its validated process.
Much of the modern standards work exists to prevent misconnection. Historically a single luer taper served many applications, which made cross-connections physically possible; the ISO 80369 series assign distinct geometries to different uses so incompatible lines simply will not mate. When you specify a connector, identifying the correct series for the application is therefore a safety decision, not just a fit decision.
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 enteral feeding flush end 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.
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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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