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SMTL Medical Disposable Datacard


Blood set with pumpchamber


All Wales Contract: Intravenous sets and related items
Sterility Status: Sterile
Usage Status: Single use
Commonly used name Blood set

 

Description

Also known as a blood administration set. Transparent tubing with retractable male luer lock at distal end, a non-vented plastic spike protected by a sheath at proximal end and 2 flexible chambers in the centre to allow manual compression. The upper chamber contains a filter (180-200µm) and the lower contains a ball which acts as a valve. A roller clamp controls the flow rate. Sets may also include a latex-free injection site.

blood set

Key areas where used

Method of use

The roller clamp is moved into its closed position and the blood or blood product container is prepared for use. If the container is rigid, an air inlet set (see air inlet datacard) should be utilised. Using an aseptic technique, the sheath is removed from the spike and inserted into the appropriate port of the container. The container is then suspended and depending on the manufacturers instructions, the double chambers are filled accordingly and the line is primed. The luer lock connector is secured to an IV cannula. Flow is regulated using the roller clamp.

Manufacturers recommend a maximum usage time of 24 hours or use in accordance with hospital policy

Presentation

Individually wrapped in a peel pouch

Sizes Required

Relevant Standards

The following standards are relevant to this product;

Organisation Standard No. Title
BSI BS EN ISO 1135: part 4: 2012 Transfusion equipment for medical use

Nomenclature

Example products

The following table lists examples of products known to be acceptable for this product description.

Brand Name Product Code Manufacturer
Blood administration set RMC2071B (4mm tubing, 200um filter) Baxter Healthcare Ltd

 


Editors

P Phillips and J Ford

Please inform SMTL of any inaccuracies noted or amendments required in this datacard.


Disclaimer

This datacard has been prepared as an aid to contracting for purchasers in the NHS in Wales, and should not be used as a substitute for literature, instructions or training from the manufacturers of the devices.

Products mentioned in this datacard are for illustration purposes only and should not be seen as an endorsement of these products.