Blood pump/gravity double chamber set with Line Label
Baxter
Injection & Infusion
Blood administration set \u2013 pump/gravity, double chamber
Certifications
CE Marked as a sterile, single Use medical device for blood administration within the European and UK markets.
Manufactured under Baxter’s quality management system, designed to comply with applicable medical device regulations and standards for infusion and transfusion sets.
Intended to meet relevant ISO and EN standards for sterile single Use transfusion equipment and tubing sets.
CE Marked as a sterile, single Use medical device for blood administration within the European and UK markets.
Manufactured under Baxter’s quality management system, designed to comply with applicable medical device regulations and standards for infusion and transfusion sets.
Intended to meet relevant ISO and EN standards for sterile single Use transfusion equipment and tubing sets.
Listed in Baxter UK price and product documentation under code MMC9609L as a blood pump/gravity double chamber set with Line Label.
Blood administration set \u2013 pump/gravity, double chamber
Description
Single-use, sterile blood pump/gravity double chamber administration set with integrated blood pump segment for use with Baxter Colleague and Evo IQ large volume infusion pumps or by gravity. The set features a flexible dual drip chamber with ball valve, 200 µm in-line blood filter, Clickluer rotary connector with Safeprime cap, integral line label and extended 225 cm tubing. It is designed specifically for the administration of red cells and other blood components using a pump where necessary, or via gravity, providing controlled flow and filtration during transfusion.
Bnefits
Dual-function design suitable for both pump-assisted and gravity blood administration using compatible Baxter Colleague and Evo IQ infusion pumps.
Flexible double chamber with ball valve helps maintain consistent drip formation and facilitates priming and flow control.
Integrated 200 µm blood filter to help remove micro-aggregates and particulate matter during blood transfusion.
Clickluer rotary connector with Safeprime cap reduces the risk of kinking and allows safe priming and connection to the patient line.
Extended 225 cm tubing provides additional reach from pump or IV pole to patient, offering flexibility in equipment and bed positioning.
Integral line label supports clear identification of the blood line in complex infusion setups, improving safety and traceability.
CE-marked sterile, single-use medical device designed for use in professional clinical environments.
Designed to be compatible with Baxter Colleague and Evo IQ pumps, helping to ensure accurate pump performance and reduce the risk of non-compatible sets.
Packaged for single-patient use to minimise cross-contamination risk and support infection prevention protocols.
Supports rapid blood administration when clinically required and used according to local transfusion policies.
Indications
Non-invasive administration of blood and blood components (e.g. packed red blood cells, plasma) in hospitals and clinical settings.
Use with Baxter Colleague and Evo IQ large volume infusion pumps for pump-assisted blood transfusion when indicated.
Use as a gravity blood administration set where gravity infusion is appropriate and pump use is not required.
Supplied non-sterilisable by user; intended for single-patient episode use only.
Packaging
Each set supplied individually sterile in a peel-open pouch or overwrap, labelled with product code MMC9609L, brand and key specifications.
Case quantities typically 50 units per carton, as indicated in Baxter UK list price documentation.
Outer cartons labelled with Baxter branding, product code, quantity, lot number, expiry date and relevant regulatory marks (including CE mark).
Packaging designed for protection in transport and storage, with clear indication of single-use status and sterility.
Usage
Use only by trained healthcare professionals familiar with local blood transfusion policies and the operation of Baxter Colleague or Evo IQ infusion pumps where pump use is required.
Check the package for integrity and expiry date before use. Do not use if the sterile barrier is damaged or the product is expired.
Using aseptic technique, open the pack and remove the set. Inspect visually to ensure there are no kinks, cracks or missing components.
Close any clamps on the line before spiking the blood bag. Attach the set spike to a compatible blood component container according to local aseptic practice.
Prime the drip chambers, filter and tubing with blood in accordance with local transfusion protocol and, if used with a pump, the pump’s instructions for use. Ensure the 200 µm filter is fully wetted and free of large air pockets.
When using as a pump set, correctly load the pump segment of the tubing into the Baxter Colleague or Evo IQ pump following the device manufacturer’s instructions, verifying that the set type and direction are correct.
Adjust flow rate using the pump controls or, in gravity mode, using clamps and drip chamber height, in line with prescribed transfusion rate and institutional policy.
Use the integral line label to identify the line clearly as a blood administration set (e.g. for red cells) and document according to local policy.
Monitor the patient and the infusion site regularly during transfusion, detecting any signs of occlusion, leakage, air in line or transfusion reaction.
At the end of transfusion, clamp the line, disconnect according to local infection prevention procedures and dispose of the entire set as clinical waste. Do not attempt to clean, re-sterilise or reuse the set.
If at any time leaks, disconnections, visible damage or malfunction are detected, stop the transfusion and replace the set in accordance with clinical judgement and local procedures.
Contraindications
Do not use if the sterile package is damaged, opened or the product is past its expiry date.
Do not reuse or re-sterilise; single-use only. Reuse may lead to infection, loss of performance and patient harm.
Not suitable for use with non-compatible infusion pumps or devices that are not designed for Baxter MMC9609L sets.
Do not use for administration of solutions or drugs that are not compatible with the materials of the set, as per local compatibility guidance.
Do not use if the line, chambers or connectors are visibly damaged, discoloured or show signs of contamination.
Do not connect to any invasive monitoring lines or devices not intended for blood administration (to avoid misconnection hazards).
Use with caution or avoid where transfusion is not clinically indicated or where gravity-only sets are recommended due to local supply guidance.
Adverse Effects
Incorrect setup, kinking or occlusion may result in under-infusion or interruption of blood delivery, potentially compromising therapy.
Incorrect loading of the pump segment in the infusion pump could lead to inaccurate flow rates or alarm conditions.
Air entry into the line due to improper priming or handling may result in air embolism if not detected and managed according to local protocols.
If used beyond recommended time limits or reused, there is a potential risk of infection or pyrogenic reactions.
Filter blockage or partial occlusion may lead to pump alarms, reduced flow or premature termination of transfusion.
Misconnection to an unintended route (e.g. mistakenly connecting to another invasive line) could cause serious patient harm if safe-connection principles are not followed.
Storage Conditions
Store in a clean, dry environment at room temperature, away from excessive heat, cold and direct sunlight.
Keep in original packaging until point of use to maintain sterility and protect from physical damage.
Avoid compression, crushing or sharp bending of cartons or pouches that could deform the tubing or components.
Store away from chemicals or solvents that could degrade plastic components or compromise packaging.
Observe any additional storage instructions on the Baxter product labelling, including temperature limits and shelf-life.
Ensure stock rotation using first-expiry-first-out (FEFO) principles to minimise the risk of using expired sets.
Duration
Intended for single-patient use over the course of a blood transfusion episode; the set should normally be used within the time limits defined by local transfusion policy (often within 4 hours of blood bag spiking) and then discarded.
Onset
Provides immediate passage of blood from the container to the patient as soon as the set is primed, connected and flow is initiated according to prescribed transfusion parameters.
