The Quad-Row Tube Clamp (TS-009) is a medical plastic component used in IV infusion sets and tubing flow control. It provides a secure, single-use connection in the fluid path and is molded from acetal (POM). Baixin Bio supplies it in standard form and with OEM/ODM customization.
Definition
The term quad-row tube clamp refers to a precision component within IV infusion sets and tubing flow control. It defines how a fluid line connects, branches, seals or regulates, and it is molded to tight tolerances so the interface performs the same way across an entire production lot.
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 Quad-Row Tube Clamp is supplied as a single-use molded part for IV infusion sets and tubing flow control. Its interface follows standard conventions so it mates predictably with compatible components, and it is produced in acetal (POM) 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 practical advantages of quad-row tube clamp cluster around safety, consistency and supply:
- 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
- Smooth fluid-contact surfaces for reliable connection
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
You will find quad-row tube clamp across a range of single-use fluid-handling assemblies, including:
- Irrigation sets
- Disposable diagnostic devices
- Syringe and pump connections
- IV infusion sets
The common thread is that every one of these settings needs junctions it can trust. A standardized, single-use component delivers that trust at scale: the same interface, the same seal and the same material behavior across an entire production lot, so the clinical team and the device maker are not relying on a one-off fitting at a critical point in the line.
How to Specify and Choose
Specifying the right part is mostly about matching a handful of variables to your assembly:
- The connection standard the mating part uses (luer slip, luer lock or a specific ISO 80369 series)
- 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
Getting these settled early means the first samples are usable and the program moves to volume faster. When a standard part does not fit, the same variables become the brief for an OEM or ODM tooling project.
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 acetal (POM) components, the practical sterilization options are 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 quad-row tube clamp 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.
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.
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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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