IV Baxter Giving Set 240cm (40) – Continu Flo Solution Administration Set
Baxter
Medical device – IV administration
IV solution administration set / giving set
Certifications
Sterile, single Use medical device (IV administration set).
Non Pyrogenic sterile fluid path, as specified for Baxter Continu Flo solution sets.
Latex Free fluid path; DEHP Containing PVC tubing as indicated for many Baxter Continu Flo sets.
Manufactured under Baxter’s quality management system compliant with applicable medical device regulations and standards (e.g. ISO Based quality systems).
Sterile, single Use medical device (IV administration set).
Non Pyrogenic sterile fluid path, as specified for Baxter Continu Flo solution sets.
Latex Free fluid path; DEHP Containing PVC tubing as indicated for many Baxter Continu Flo sets.
Manufactured under Baxter’s quality management system compliant with applicable medical device regulations and standards (e.g. ISO Based quality systems).
IV solution administration set / giving set
Description
The IV Baxter Giving Set 240cm (40) is a sterile, single-use Continu-Flo solution administration set designed for intravenous infusions. It features approximately 240 cm of tubing, a non-return (backcheck) valve to help prevent backflow, and two Y-port injection sites positioned high and low on the line for convenient medication boluses or additive injections. A high-quality V-track flow controller enables accurate manual regulation of infusion rates. Each individual set is supplied sterile in a peel-open pack and is intended for use by trained healthcare professionals, commonly in hospital, clinic and aesthetic/IV vitamin therapy settings.
Bnefits
Provides a dedicated IV solution administration line for controlled infusion of fluids, vitamins and medications.
Continu-Flo design with backcheck (non-return) valve helps prevent backflow from secondary containers or the patient line.
Two Y-port injection sites (high and low) allow intermittent drug or vitamin injections without disconnecting the primary line.
Approximate 240 cm tubing length offers flexibility and ease of positioning of the infusion pump or IV pole relative to the patient.
High-quality V-track controller allows manual adjustment of flow rate for gravity infusions.
Single-use, sterile fluid path reduces risk of cross-contamination between patients.
Designed to be compatible with Baxter Continu-Flo systems and commonly used infusion pumps and IV poles.
Supplied as a box of 40, making it suitable for clinical and aesthetic practice stock management.
Indications
Intravenous administration of crystalloids, colloids and compatible solutions.
Infusion of IV vitamins, minerals and nutritional solutions in aesthetic, wellness and medical settings when prescribed by a healthcare professional.
Administration of compatible IV medications via primary infusion or through the integrated injection sites.
Situations where a long (approximately 240 cm) IV giving set is required to allow flexibility of equipment positioning relative to the patient.
Medical-grade flexible tubing (PVC with DEHP, typical of Baxter Continu-Flo sets).
Non-vented spike for connection to IV solution containers (bottles or bags).
Drip chamber for visual monitoring of flow and drop rate.
Integrated backcheck (non-return) valve in the fluid path.
Two Y-port injection sites (typically Clearlink/Interlink or equivalent needle-free/needle-accessible ports) positioned high and low on the line.
V-track (roller-type) flow controller for manual regulation of infusion rate.
Male Luer lock adapter at the patient end for secure connection to IV cannula or extension set.
Latex-free fluid path components (typical of modern Baxter Continu-Flo sets).
Formulation
Sterile, single-use IV solution administration set (Continu-Flo technology) with approximately 240 cm tubing.
Non-vented spike, drip chamber, backcheck valve, two Y-port injection sites (high and low), V-track controller and male Luer lock adapter.
DEHP-containing PVC tubing with latex-free fluid path; non-pyrogenic and sterilised (e.g. by radiation or ethylene oxide) as per Baxter Continu-Flo product family.
Packaging
Each giving set is individually sterile-packed in a sealed medical-grade pouch.
Labeling typically includes product name, length, brand (Baxter), lot number, expiry date and sterilisation/single-use symbols.
Usage
For use only by trained healthcare professionals in accordance with local protocols and the instructions-for-use supplied by Baxter.
Verify integrity of the sterile package and expiry date before use; do not use if the pouch is opened, torn or damaged.
Close the V-track (flow) controller before spiking the solution container.
Remove protective cap and insert the spike aseptically into the IV fluid container (bag or bottle), ensuring a secure fit.
Squeeze and partially fill the drip chamber to the recommended level to allow visual monitoring of drops.
Prime the line by slowly opening the V-track controller until all air is expelled and the tubing is completely filled with fluid, then close the controller.
Connect the male Luer lock adapter at the distal end of the set to the patient’s IV cannula or extension set, ensuring a secure Luer-lock connection.
Adjust the V-track controller to achieve the prescribed infusion rate for gravity infusions or connect to a compatible infusion pump if being used under pump control.
Use the Y-port injection sites (high or low) as indicated to administer compatible medications or vitamins, following aseptic technique and institutional protocol.
Do not reuse; discard the entire giving set after completion of the prescribed infusion, following local clinical waste regulations.
Contraindications
Do not use if the sterile package is opened, damaged or past its expiry date.
Not to be reused or resterilised; reuse may increase the risk of infection and device malfunction.
Do not use for solutions or medications that are contraindicated for administration via PVC/DEHP-containing tubing or via Continu-Flo sets.
Do not use if visible damage, kinks or occlusions are present in the tubing, connectors, drip chamber or injection sites.
Use only with compatible solutions, containers and infusion pumps as per Baxter and institutional guidelines.
Adverse Effects
As with any IV administration set, improper use may contribute to complications such as infection, phlebitis, infiltration, air embolism or fluid overload.
Incorrect priming or failure to remove air from the line may result in air entering the patient’s circulation.
Use with incompatible solutions or medications may lead to precipitation, tubing damage or reduced drug efficacy.
Re-use or use of a compromised sterile pack may increase risk of cross-contamination or infection.
Storage Conditions
Store in a clean, dry environment at room temperature, away from direct sunlight and excessive heat.
Keep in original packaging until immediately before use to maintain sterility.
Do not use after the expiry date printed on the pack.
Avoid crushing, bending or storing under heavy objects that may deform the tubing or components.
Duration
The giving set itself is used for the duration of a single IV infusion episode and must be discarded after use; duration of treatment (minutes to hours) is determined by the prescribed IV therapy protocol, not by the set.
Onset
Not directly applicable to the device; onset and clinical effect depend on the medication or fluid being infused rather than the giving set itself.
