Volumetric IV Infusion Pump with Alarm System & Rechargeable Battery
$869.44
Description
Bring infusion information and controls together with this volumetric IV infusion pump with a 2.8-inch TFT-LCD display, alarm system and built-in rechargeable lithium battery. The front panel combines a status display and physical keys beside the infusion-set compartment, while the pictured carrying handle and rear pole clamp support planning its placement within an established clinical workflow.
The listed flow-rate range is 1–699 mL/h. Alarm functions cover occlusion, air bubbles, an open door and motor failure, with adjustable pressure thresholds. These are equipment features for evaluation by a trained healthcare team, not a guarantee of a particular clinical outcome or suitability for every infusion.
For purchasers already familiar with the manufacturer's brand and the SP750 model. Confirm the intended use, approved IV sets, calibration requirements and facility procedures with the responsible clinical team before ordering. This listing is not an introductory guide to administering fluids or medication. Contact us for destination and supply review.

Why This Infusion Pump
- Front-panel information: The display presents rate, volume and time information as illustrated, with physical controls alongside the infusion compartment.
- Multiple alarm conditions: Listed indications cover occlusion, air bubbles, door opening and motor failure for review within the facility's response procedures.
- IV-set calibration capability: The listed calibration function requires the correct manufacturer procedure and approved set selection; it does not make every IV set compatible.
- Power flexibility: AC/DC operation and a rechargeable lithium battery give the team power arrangements to evaluate within its continuity and checking procedures.

What Is It For & How It Helps
This is fluid-administration equipment for use by appropriately trained healthcare personnel within the manufacturer's intended use. Selection of treatment, fluid, rate and monitoring requirements belongs to the responsible clinical team, not to a product listing.
Before procurement, review the manufacturer's full instructions, approved IV sets, commissioning and calibration requirements, alarm behaviour and maintenance arrangements. A listed flow range is an equipment specification, not a recommended treatment rate.
Plan a stable installation with visible controls, accessible power connections and an unobstructed infusion compartment. Follow facility procedures for patient monitoring, alarm response and alternative arrangements if equipment fails. Neither an alarm nor a battery replaces direct professional oversight.
Infusion Pump Specifications
| Device | Volumetric IV infusion pump |
|---|---|
| Listed flow-rate range | 1–699 mL/h |
| Display | 2.8-inch TFT-LCD |
| Operation | Physical keypad |
| Listed alarm conditions | Occlusion, air bubble, door open and motor failure |
| Pressure thresholds | Adjustable |
| Listed control functions | Anti-bolus system and automatic stop during alarms; follow the supplied instructions |
| Power | AC/DC operation; built-in rechargeable lithium battery |
| Pictured hardware | Carrying handle and rear pole clamp |
Confirm the supplied accessories, compatible power connections and approved IV-set configuration before ordering.
Tips & Suggestions

Reviewing procurement requirements
Have the clinical and equipment-management teams review the intended use and model documentation before purchase. Confirm that commissioning, service support and the required consumables can be arranged for your facility.
Checking IV-set requirements
Compare the manufacturer's approved-set and calibration instructions with the sets your facility uses. Do not treat broad supplier compatibility wording as permission to use an unapproved set.
Planning installation
Review the mounting hardware, support requirements and access around the device. Arrange the station so trained personnel can see the screen and reach controls without straining cables or tubing.
Preparing staff training
Establish supervised familiarisation with the supplied instructions and facility procedures before clinical use. Knowledge of the brand does not replace training for the exact model and approved configuration.
Reviewing alarm response
Make sure responsible staff understand the documented alarm indications and response procedures. Assess alarm visibility and audibility within your actual work area rather than relying on a feature list alone.
Planning power continuity
Review power requirements, battery checking and charging procedures before introducing the unit into service. Maintain the facility's alternative arrangements for power or equipment failure rather than assuming battery operation is uninterrupted.
Organising maintenance records
Keep commissioning, inspection and service records within your equipment-management process. Follow manufacturer guidance for cleaning and maintenance, and remove damaged equipment from use through the facility's procedure.
Not Ideal For
Not for unsupervised self-treatment or buyers unfamiliar with the manufacturer's brand and this model who need introductory selection guidance. Do not assume universal IV-set compatibility, uninterrupted battery operation or that alarm and anti-bolus features eliminate clinical risk.
Frequently Asked Questions
What is the listed flow-rate range?
The listed range is 1–699 mL/h. This is an equipment specification, not a treatment recommendation; clinical settings must be determined by the responsible healthcare team.
Can any IV set be used?
Do not assume universal compatibility. Review the manufacturer's approved IV sets and calibration instructions with the responsible clinical or equipment-management team before purchase and use.
Which alarms are listed?
Listed alarm conditions include occlusion, air bubbles, an open door and motor failure, with adjustable pressure thresholds. Follow the manufacturer's instructions and facility response procedures.
How is the pump powered?
It supports AC/DC operation and has a built-in rechargeable lithium battery. Review the supplied power, charging and battery-checking instructions; do not assume uninterrupted operation.
Should I contact you before ordering?
Yes. Contact us for destination and supply review and confirm the model and accessory configuration. Purchase only if you are already familiar with the manufacturer's brand and this model and have confirmed suitability with the responsible healthcare team.
Important Notices & Disclaimers
Buyer familiarity required: Intended for purchasers already familiar with the manufacturer's brand, the SP750 model and its operating requirements. Review the manufacturer's documentation and confirm suitability with the responsible healthcare team before ordering.
For appropriately trained healthcare personnel within the manufacturer's intended use and facility procedures. This listing does not provide dosing, infusion programming or clinical treatment instructions. Alarm and anti-bolus functions do not replace professional supervision or eliminate risk.
Follow supplied instructions for approved IV sets, calibration, commissioning, electrical safety, battery care, cleaning and maintenance. Do not immerse the device or treat it as waterproof. Stop use and follow facility procedures if equipment or accessories appear damaged.
Destination review: Products may be restricted in some countries. Contact Très Elite through the official contact form before ordering, or submit an order for destination feasibility review. Orders that cannot be supplied will be cancelled. Uncaptured authorisations may be voided where applicable; collected payments require refund handling. Temporary bank authorisation holds may appear.
Shipping & Delivery
Destination and order checks
Contact us for destination and supply review before ordering. Check your full address including unit and postal code, recipient/contact details, selected model, design, dimensions, accessory contents and intended quantity. Read Quick Answers (Order & Shipping FAQs) on the product listing.
Processing and delivery methods
Most standard orders require approximately 3–7 business days of processing before shipment; carrier transit is additional. Product-specific estimates take priority. Standard is not express. Express, where offered, shortens transit but does not bypass sourcing, preparation or order review, or guarantee an event date. See Shipping & Handling and review the estimate for your selected method and destination.
For standard holiday delivery, plan at least 2–3 weeks ahead with additional peak buffer and any longer product-specific estimate. This is planning guidance, not an arrival guarantee.
Correction requests within 60 minutes
Report address, recipient/contact, product/variant, size, colour or quantity errors through the official contact form or website live chat within 60 minutes of ordering, including weekends and holidays. Timely requests do not guarantee correction because processing may already have begun. Do not rely on replies to automated order emails.
International shipping and customs
VAT, customs and duties treatment varies by destination, product, carrier and shipping arrangement. Where expressly identified as duties prepaid/DDP, included import charges are handled in advance; otherwise recipient charges may apply and customs may request documentation. See International Shipping or ask through the official contact form.
Arrival inspection and returns
Report damage, defects or incorrect supply through the official contact form with order details, clear photographs and a clear video showing the issue. Retain the item and packaging; do not return without approval. Change-of-mind and customer selection errors are normally ineligible under the published terms; discretionary approval may apply. This does not replace assistance for damage, defects or fulfilment errors. Review Returns & Exchanges and Contact Us.
Device features and sample screen values are not treatment instructions, performance guarantees or destination authorisation. Follow supplied instructions and applicable store policies.

