Buretrol gravity blood/IV administration set with burette
Certifications
Marked as a CE Class I medical device in EU/UK product listings, indicating conformity with applicable European medical device regulations.
Manufactured by Baxter Healthcare, a global medical device and pharmaceutical company operating under recognised quality management systems for medical devices.
Distributed in the UK by registered medical device and medicines wholesalers (e.g. Medisave UK Ltd, 3S Healthcare) operating under MHRA oversight where applicable.
Marked as a CE Class I medical device in EU/UK product listings, indicating conformity with applicable European medical device regulations.
Manufactured by Baxter Healthcare, a global medical device and pharmaceutical company operating under recognised quality management systems for medical devices.
Distributed in the UK by registered medical device and medicines wholesalers (e.g. Medisave UK Ltd, 3S Healthcare) operating under MHRA oversight where applicable.
Buretrol gravity blood/IV administration set with burette
Description
The Buretrol Gravity Administration Set (VCM0172P / TRC0172P) is a Baxter Buretrol solution administration set incorporating a 150 ml burette for gravity infusion. It features a ball valve vented spike chamber with a 60 drops per mL (60 DPM) drip rate, a 15 µm in-line filter, a needle Y-injection site and a Clickluer/rotary male luer connector with hydrophobic (Safeprime) cap on 240 cm tubing. The set is designed for controlled administration of IV solutions and blood products, particularly where precise volume limitation and visual monitoring of infused volume are required.
Bnefits
150 ml burette enables accurate measurement and control of infused volume, useful in paediatric and fluid-restricted patients.
Gravity Buretrol solution set with ball valve vented spike and 60 DPM chamber supports consistent drip-rate control during gravity infusions.
Integrated 15 µm filter helps retain particulate matter in IV solutions, supporting safer infusion practice.
Needle Y-injection site allows addition of compatible medications or fluids into the line according to clinical protocols.
Clickluer rotary male luer connector with hydrophobic/Safeprime cap provides a secure connection to vascular access devices and helps minimise leakage and air entry.
240 cm tubing length offers flexibility in positioning solution containers relative to the patient bed or treatment chair.
Single-use, sterile set simplifies setup and reduces cross-contamination risk when used according to instructions.
Indications
Gravity administration of IV solutions where a burette is required to limit and monitor infused volume.
Controlled administration of blood and blood components when used according to local transfusion policies and Baxter’s instructions for use.
Use in paediatric, neonatal, critical care and other clinical settings requiring close monitoring and precise control of infusion volumes.
General hospital and clinical IV therapy when a burette set with integrated filter and Y-site is indicated.
150 ml transparent burette body with integrated ball valve vented spike chamber (60 drops/mL).
15 µm in-line filter located in the chamber/upper set section for particulate retention.
Needle Y-injection site along the tubing for medication/additive administration.
Clickluer rotary male luer connector with hydrophobic (Safeprime) cap at the distal end.
Approx. 240 cm length IV tubing manufactured from medical-grade polymers (e.g. PVC) suitable for IV solution and blood administration (exact polymer formulation not stated in open product literature).
Formulation
Non-medicated, non-pharmacological, single-use sterile IV administration set with burette, intended as a medical device accessory for IV and blood administration.
Packaging
Supplied individually (Pack size: 1 set) as a sterile, single-use Buretrol gravity administration set.
Each unit is individually packaged to maintain sterility until point of use, labelled with product code TRC0172P / VCM0172P, volume (150 ml burette), length (240 cm), drop rate (60 DPM) and manufacturer/brand information.
Usage
For use only by trained healthcare professionals, following institutional IV therapy and, where applicable, transfusion protocols.
Inspect the outer packaging and the set before use; do not use if packaging is damaged, opened or if any component appears compromised.
Close all clamps on the set prior to spike insertion.
Using aseptic technique, insert the vented spike into the IV solution or blood container and open the vent as required for glass or rigid containers.
Prime the burette by opening the appropriate clamp and filling it to the desired volume (up to 150 ml); close the clamp once the required volume has been reached.
Prime the drip chamber, filter and downstream tubing by allowing fluid to run until all air is expelled and the filter and line are fully wetted; then close the clamp.
Connect the rotary male luer to the patient’s vascular access device securely, ensuring connections are tight and leak-free.
Adjust the drip rate using the roller clamp or appropriate flow control device, using the 60 DPM chamber as a reference, and monitor the patient and infusion regularly.
If using the needle Y-injection site, disinfect the site according to protocol before injecting compatible medications or additional fluids; verify compatibility with the primary solution.
Use the burette to limit and document infused volume according to prescribing instructions, refilling the burette as needed while observing maximum prescribed volumes.
After completion or when the set is no longer required, clamp the line, disconnect from the patient according to institutional policy and dispose of the entire set as clinical waste; do not reuse or resterilise.
Contraindications
Do not use if the package is opened, damaged, or if sterility is in doubt.
Do not reuse or resterilise; the set is intended for single-patient, single-use only.
Not intended for infusion of solutions that are incompatible with the materials of the set (refer to Baxter’s compatibility information and institutional protocols).
Use only for gravity administration; do not use with infusion pumps unless explicitly authorised and listed as compatible in Baxter’s pump-set compatibility documentation.
Adverse Effects
Potential complications relate to IV therapy and blood administration in general (e.g. infiltration, phlebitis, infection, air embolism, fluid overload, transfusion reactions) and depend on clinical use rather than the administration set alone.
Improper priming or setup could contribute to air entry or inaccurate fluid delivery if standard IV procedures are not followed.
Failure to adhere to local transfusion and IV guidelines can increase the risk of therapy-related complications.
Storage Conditions
Store in a clean, dry environment at room temperature, away from direct sunlight and excessive heat.
Keep the product in its original packaging until immediately before use to maintain sterility and protect from contamination or mechanical damage.
Do not expose packaging to sharp objects or heavy loads that could crush or puncture the burette chamber or tubing.
Keep out of reach of children and unauthorised personnel.
