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Infusion Pump

Infusion Pump HepoFusion I2

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Infusion Pump HepoFusion I2
Product data

Technical specifications

Key specifications and configuration details for Infusion Pump HepoFusion I2

Consumables
Universal consumables
Heating
External heating
Preset Volume Error
Preset volume error ≤±5%
Nutrition Modes
Nutrition, volume, first dose, total volume, micro, drip rate and neonatal modes
Display Type
Capacitive touchscreen
Display Size
4.3-inch
Preset Volume Increment
Minimum increment of 0.01ml
Power Supply
AC power and built-in battery
Weight
≤1.45Kg
Dimensions
160mm×171mm×200mm
FAQ

Frequently asked questions about Infusion Pump HepoFusion I2

Answers to common questions about product selection, use, and support.

What is the intended use of the HepoFusion I2 nutrition pump?
Used with infusion sets for the intravenous administration of medicinal fluids and blood to patients; not for the infusion of analgesics, chemotherapeutic agents or insulin. Used with enteral nutrition administration sets to deliver nutrient solutions to the patient's gastrointestinal tract in an adjustable manner in hospitals.
What are the overall functions of the HepoFusion I2?
During operation of the infusion pump, sensors including the line pressure sensor, air-in-line sensor, drip sensor, temperature sensor and motor speed sensor continuously monitor the operating status of the pump; when an abnormal condition occurs, the pump immediately alarms and stops.
How is the HepoFusion I2 installed?
The main unit of this product is fully assembled. Mount the main unit on an infusion stand or place it on a stable tabletop, connect the supplied accessories to the main unit, plug the warming device into the warming socket and the drip sensor into the drip interface. The warming device and silicone heating tube are optional accessories.
How should alarms on the HepoFusion I2 be resolved?
When an alarm occurs, first check the patient's condition. When the infusion pump alarms, take the corresponding measures according to the following steps: 1. Check the patient's condition; 2. Confirm the parameter or type that is alarming; 3. Identify the cause of the alarm; 4. Clear the alarm; 5. Check whether the alarm has been resolved.
How should the HepoFusion I2 battery be maintained?
The HepoFusion I2 is equipped with a rechargeable lithium battery so that the device can operate normally when no external power supply is available. The pump can switch between external power and battery power without interrupting operation; when connected to an external power supply, the pump gives priority to external power.

Compliance Notice

This product is a medical device certified under NMPA, CE, ISO13485. It shall only be used by professional medical personnel in accordance with user manual and local regulations. Not for self‑diagnosis or self‑treatment. All information is for product display only, not medical advice.

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