Adfusion Hemodialysis Blood Tubing Set
Pack Sizes Available
Product Description
Technical Specifications
- Brand and Compatibility: ADfusion blood tubing set — distributed from India; compatible with Fresenius, B. Braun, Campbell, Baxter, Nikkiso, Nipro, Gambro, Bellco hemodialysis machines; universal dialyzer connector
- Set Components: Arterial line (red-coded) + Venous line (blue-coded); drip chambers on both lines (anti-foaming, air-eliminating); colour-coded ergonomic clamps; injection ports; Luer-lock connectors; transducer protectors included
- Tubing Material: Medical-grade PVC; kink-resistant; smooth inner wall to reduce haemolysis and bubble generation; non-DEHP formulations available on request; biocompatible and hemocompatible
- Sterilization: Ethylene oxide (EO) sterilized; single-use only; non-toxic; pyrogen-free; individually sealed per unit
- Priming Volume: Typical total priming volume: 70–120 mL depending on configuration (arterial + venous + drip chambers); blood pump segment internal diameter: standard 6.35mm (Fresenius compatible) or alternate diameters available per machine specification
Frequently asked questions
The Adfusion Hemodialysis Blood Tubing Set is confirmed compatible with Fresenius, B. Braun, Campbell, Baxter, and Japan-brand hemodialysis machines. The universal design also covers most other commonly used dialysis machines including Nikkiso, Nipro, Gambro, and Bellco configurations. Because dialysis units in many international markets run mixed machine fleets rather than a single brand, universal compatibility is a significant procurement advantage — it eliminates the need to stock separate tubing SKUs for each machine type in the same centre.
Every hemodialysis blood tubing set consists of two main components. The arterial line (typically red-coded) connects the patient's vascular access — an AV fistula needle or central venous catheter — to the inlet port of the dialyzer. It draws blood out of the patient toward the dialysis machine. The venous line (typically blue-coded) connects the dialyzer outlet port back to the patient's vascular access, returning the treated blood after it has passed through the dialyzer membrane. The two lines together form the extracorporeal circuit through which blood travels outside the body during every hemodialysis session.
Drip chambers are transparent reservoirs built into both the arterial and venous lines. They serve several functions. They provide a visible fluid level that allows the dialysis nurse to confirm appropriate filling and detect air in the circuit during priming. The arterial drip chamber is typically filled to approximately 90% during setup. The design of the chamber also reduces foaming during priming — foam in the circuit traps air bubbles that can trigger the machine's air detector alarm and interrupt treatment. Well-designed drip chambers that minimise foaming reduce setup time and the incidence of false air detector alarms during sessions.
EO sterilized means the set has been sterilized using ethylene oxide gas, a process that kills all microorganisms including bacterial spores without degrading the PVC tubing material. It is the standard sterilization method for heat-sensitive disposable medical devices that come into contact with blood. Pyrogen-free means the product contains no pyrogens — bacterial endotoxins or other fever-inducing contaminants — which is a mandatory safety standard for any device where blood or IV fluids pass through the material. Both designations are required for regulatory approval of dialysis bloodline sets in all major markets.
The Adfusion Hemodialysis Blood Tubing Set is confirmed in a pack of 25 units for export and institutional procurement, with alternate configurations of 30 units per box also available for certain machine-specific variants. Each set is individually sterile packaged. For large-volume wholesale orders, Sara Wellness supplies case quantities and can accommodate combined orders covering multiple dialysis consumable SKUs — including AVF needles and transducer protectors — within a single export shipment.
Blood tubing sets are strictly single-use medical devices. Reuse creates risks on multiple fronts. Residual blood proteins in the tubing from a previous session degrade and create pyrogen contamination risk for the next patient. The tubing material undergoes stress during the pump segment's mechanical compression and cannot reliably maintain its structural integrity through a second session. Infection transmission risk between patients using the same bloodline — even after cleaning attempts — is a real and documented complication of bloodline reuse in under-resourced dialysis programmes. All international dialysis guidelines, including those from the KDOQI and the ERA/EDTA, mandate single use of all blood circuit components.
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