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Pre-owned
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BD Alaris NeXus CC Syringe Driver Mfd. 2022
£349.99
This item
CME Bodyguard 323 Colour Vision Infusion Pump - New in Box
£199.99
The BD Alaris neXus CC is a precision syringe pump for controlled delivery of fluids, medications, parenteral nutrition and blood products across adult, paediatric and neonatal populations. It takes 5 ml to 50 ml Luer lock syringes and runs flow rate, volume over time, dose calculation and preconfigured protocol modes. Its defining capability is online pressure monitoring: SMART detection identifies whether a pressure sensing disc extension set or a standard set is fitted, giving early occlusion detection and reducing post-occlusion bolus risk. Guardrails hard and soft limits operate against institution-defined thresholds without needing a permanent network connection. This unit is dated 2022.
| Item | Detail | Condition |
|---|---|---|
| Alaris neXus CC syringe pump | BD syringe pump, 2022 unit, with internal NiMH battery fitted | USED |
| Mains lead | AC power lead for the pump | USED |
| Item | Detail | Status |
|---|---|---|
| Syringes | Approved three-piece Luer lock syringes, 5 ml to 50 ml | SOLD SEPARATELY |
| Pressure disc extension sets | Sets required for online pressure monitoring | SOLD SEPARATELY |
| Standard extension sets | Sets for conventional occlusion detection | SOLD SEPARATELY |
| Gateway Workstation | Docking workstation for multi-pump working | SOLD SEPARATELY |
| MRI Capsule | Enclosure for continuity of infusion during imaging | SOLD SEPARATELY |
| Syringe lock box | Only for use when the pump is docked to a Gateway Workstation | SOLD SEPARATELY |
| Pole clamp and mounting hardware | Drip stand or rail mounting | SOLD SEPARATELY |
| Drug library dataset | Institution-specific Guardrails dataset and its deployment | SOLD SEPARATELY |
| Service and calibration | Engineer service, performance verification and certification | SOLD SEPARATELY |
Checked before dispatch
These are in-house workshop checks. Damaged or non-working items are not dispatched. This item may require service and calibration. A full engineer service and calibration is not included unless this listing states that the unit has been serviced. Delivery accuracy verification, planned maintenance and periodic electrical safety testing remain with the operating organisation once the pump is in service.
Clinical use
| Manufacturer | BD, Becton, Dickinson and Company |
| Model | Alaris neXus CC |
| Device type | Syringe infusion pump |
| Year of manufacture | 2022 |
| Patient population | Adult, paediatric and neonatal |
| Syringe compatibility | 5 ml to 50 ml Luer lock, approved single-use three-piece syringes |
| Flow rate accuracy | Plus or minus 2 per cent at 25 ml/h, per IEC 60601-2-24 |
| Pressure monitoring | L0 to L10, 50 to 1000 mmHg, 11 levels |
| Drug library capacity | 3,000 setups across 30 profiles |
| Battery type | NiMH rechargeable, changeable at service |
| Battery life | Up to 6 hours at 5.0 ml/h |
| Battery recharge time | 2.5 hours from discharge to 90 per cent |
| Mains power supply | 115 to 230 V AC, 50 to 60 Hz, 10 VA nominal |
| Dimensions, W x H x D | 335 x 121 x 200 mm |
| Weight | 2.4 kg |
| Ingress protection | IP32, IP33 with AC power cable retainer kit |
| Connectivity | Wi-Fi, RS232, nurse call |
| Standard compliance | IEC 60601-2-24 |
| Condition | Pre-owned |
| Component | Action | Interval |
|---|---|---|
| Syringe carriage and plunger grip | Inspect for residue, free movement and secure hold on the plunger flange | Before each use |
| Alarms | Confirm audible and visual alarms operate at power-up self test | Before each use |
| Battery | Return to mains after use, check the charge indicator and note any drop in runtime | After each use |
| Housing, keypad and display | Wipe down per local policy, inspect for cracks, fluid ingress and worn legends | Between patients |
| Mains lead and plug | Inspect for damage, strain at the entry point and secure retention | Weekly |
| Drug library | Confirm the loaded dataset and profile match the current institutional version | Per local policy |
| Performance verification and electrical safety test | Engineer service, delivery accuracy check and calibration | Per local schedule |
The above is general guidance. The manufacturer instructions for use and the operating organisation's medical device management policy take precedence. Any pump showing a fault, an unexplained alarm pattern or a suspected accuracy problem should be taken out of service until it has been tested.
Orders shipped outside the United Kingdom may attract import duty and local tax, which are charged by the destination country and are the buyer's responsibility.
SelfiMed offers a 30-day change-of-mind return policy on eligible items. To request a return, please contact us within 30 days of delivery. Items returned under this policy must be in the same condition as received and suitable for resale.
Please note that brand new items must remain unopened, unused and in their original packaging to be eligible for return. Once a new item has been opened or used, it may no longer qualify for return as new, and any accepted return may be subject to restocking fees.
For hygiene reasons, opened CPAP masks, CPAP parts and CPAP accessories, including tubing, filters and humidifier chambers, cannot be returned.
Return shipping costs are the responsibility of the customer.
This does not affect your statutory rights.
Refunds are issued to the original payment method once the returned item reaches us and has been checked, normally within five working days.
Faulty items are refunded in full, including the delivery you paid.
SelfiMed Ltd, trading as SelfiMed UK, supplies medical equipment, replacement parts and accessories but does not provide medical advice, diagnosis or treatment. Customers are responsible for ensuring that they are legally authorised to purchase and use any equipment supplied and for complying with all applicable regulations in their country. Certain medical devices may require a valid prescription or clinical directive before dispatch. Components, accessories and kits are supplied as replacement or accessory items unless expressly stated otherwise, and correct assembly, calibration, commissioning and application remain the responsibility of the user or an appropriately qualified professional.
All equipment must be used, maintained and cleaned in accordance with the manufacturer’s instructions. SelfiMed UK accepts no liability for misuse, incorrect assembly, mishandling, unauthorised modification or use outside the manufacturer’s intended purpose, and does not guarantee suitability for any particular clinical outcome unless confirmed in writing. Pre-owned or refurbished equipment should not be used for emergency or critical care without appropriate professional oversight and commissioning. Customers should obtain advice from a qualified healthcare professional or medical device technician where required and assume responsibility for the lawful, safe and appropriate use of the products purchased.
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