BD Alaris™ neXus GP Volumetric Pump
Overview
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Conditions for Use
The BD Alaris™ neXus GP Volumetric Pumps are restricted medical devices intended for use by qualified, trained personnel
to deliver either continuous or intermittent infusion therapy of:
• Fluids
• Medications
• Nutritional supplements
• Blood and blood products
Indications
The BD Alaris™ neXus GP Volumetric Pumps are indicated for delivery of therapies through the following clinically
acceptable routes
• Intravenous (IV)
• Subcutaneous
• Irrigation of fluid spaces
Contraindications
The BD Alaris™ neXus GP Volumetric Pump is contraindicated for enteral or epidural therapies .
Undesirable Side-Effects
The BD Alaris
™
neXus GP Volumetric Pump has no undesirable side-effects associated with its use when used in
accordance with the Directions for Use .
Compatibility
The BD Alaris™ neXus GP Volumetric Pump is compatible with the following:
• The Alaris™ Gateway Workstation v1 .3 .x and v1 .6 .x – see ‘Associated Products’
• Standard, single-use, disposable infusion sets – see ‘Infusion Sets’
• The Active RFID asset tag supplied by BD with this Pump
• The following minimum versions of software products are also compatible – see ‘Products and Spare Parts’
-
BD Alaris™ neXus Editor v5 .0
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BD Alaris™ neXus Transfer Tool v5 .0
-
BD Alaris™ Technical Utility v2 .0
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BD Alaris™ Communication Engine v 2 .0
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BD Alaris™ CQI Event Reporter V4 .4