Baxter Blood Administration Set

Baxter Blood Administration Set

Baxter

Injection & Infusion
  • Manufactured by Baxter Healthcare, a major regulated medical device company supplying sets globally.
  • Conforms to standard specifications for single Use blood administration/transfusion sets (sterile, disposable, with blood filter and non Vented spike) as per clinical transfusion practice guidelines.
Blood transfusion/administration set

Description

The Baxter Blood Administration Set is a sterile, disposable transfusion set designed for the safe administration of whole blood or blood components via gravity. It features transparent tubing of 4.04 mm internal diameter, a non-vented spike protected by a sheath for bag access, two flexible drip chambers (upper chamber with a 180-200 µm blood filter, lower chamber containing a ball-valve for flow regulation), a roller clamp for flow control, and a male luer lock connector. Supplied as a box of 50 single-use sets, it enables reliable and controlled blood transfusion in hospital and clinical settings.

Bnefits

  • Integrated 180–200 µm filter helps remove micro-aggregates and small clots, enhancing transfusion safety.
  • Ball-valve drip chamber design provides controlled flow and reduces air embolism risk.
  • Large internal diameter tubing (4.04 mm) permits adequate flow rate for blood transfusion.
  • Non-vented spike and protected sheath help maintain sterility during bag spike insertion.
  • Single-use, sterile and disposable — reduces cross-contamination and infection risk compared to reusable sets.

Indications

  • Transfusion of whole blood or blood components (red cells, plasma, platelets) in hospital or clinical settings.
  • Use whenever safe, filtered, gravity-based administration of blood/blood products is required.
  • Suitable for general wards, intensive care units, emergency departments, blood banks and transfusion services.

Composition

  • Medical-grade PVC or PVC-blend tubing (internal diameter ~4.04 mm).
  • Plastic non-vented spike (polypropylene or similar) with protective sheath.
  • Drip chamber(s) made of transparent medical-grade plastic.
  • Blood filter membrane rated 180–200 µm inside upper chamber.
  • Ball-valve assembly in lower chamber to prevent backflow or air aspiration.
  • Roller clamp made of medical-grade plastic for flow regulation.
  • Male Luer lock connector (polypropylene or similar) at distal end.

Formulation

  • Sterile, single-use, non-vented gravity blood administration set with integrated blood filter and drip-chamber design.
  • Tubing length and internal diameter engineered for optimal flow of blood and components.
  • Set intended for manual gravity-based flow; no pump required when used per instructions.

Packaging

  • Box containing 50 individually packaged sterile blood administration sets.
  • Each set supplied sterile, individually wrapped/blister-packed and labelled with product code (TRMMC2071B), batch number and expiry date.

Usage

  • Inspect packaging for integrity and expiry date before use.
  • Use aseptic technique: spike the blood bag using the non-vented spike with protective sheath, ensuring sterility.
  • Prime the tubing gently to expel air before connecting to the patient’s IV access.
  • Use the roller clamp to control and regulate flow rate as required by transfusion protocol.
  • Monitor the drip chamber and filter; ensure the filter and valve function correctly throughout the transfusion.
  • Discard the set after a single use according to biohazard waste disposal protocols.
  • Do not reuse or attempt to re-sterilise the set.

Contraindications

  • Not for use with non-blood fluids requiring a vented or pump-compatible administration set.
  • Not suitable if packaging is damaged or sterility is compromised.
  • Not to be reused — single-use only.
  • Not compatible with infusion pumps that require vented or non-filter sets, unless validated by manufacturer.

Adverse Effects

  • Risk of air embolism if tubing is not primed properly before transfusion.
  • Potential hemolysis or blood cell damage if flow rate is too high or set is incorrectly used.
  • Allergic or sensitivity reactions if patient is sensitive to PVC or plasticiser (rare).
  • Risk of contamination/infection if aseptic technique is not strictly followed or set is reused.

Storage Conditions

  • Store in a dry, cool place away from direct sunlight and excessive heat or cold.
  • Keep in original sealed packaging until use to maintain sterility.
  • Avoid exposure to sharp objects or conditions that might damage packaging or tubing integrity.

Duration

Onset

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