Secondhand Akas Infumax Infusion Pump

Objective AI Report

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Report date: 12.11.2025

AKAS Infumax Infusion Pump Analysis Report

Device Description and Purpose of Use

The product in the image is an infusion pump that enables the controlled and precise intravenous administration of substances such as fluids, medications, or nutrients to patients in medical settings. The device is particularly used in areas such as intensive care, general wards, oncology, and anesthesia. It is understood from the buttons on it that it is suitable for use in both adult (Adult) and pediatric (Pedia) patients.

Brand and Model Identification

The brand of the device is AKAS, clearly visible on the upper and lower parts of the front panel. The model of the device has been identified as Infumax, also written on the front. The device is a volumetric infusion pump known as AKAS Infumax.

General Condition and Physical State

The overall condition of the product appears good and well-maintained. No major physical damage, cracks, or significant color fading have been observed in the visuals. The device casing is clean, and there is no significant deformation other than minor signs of use. The device is in working condition; its screen and indicator lights are active, which suggests that its electronic components are functional.

Technical and Mechanical Analysis

Upon visual inspection of the device’s mechanical and electronic components, the following details have been identified:

• Mechanical Components: The front cover where the infusion set is attached and the blue-colored mechanism appear robust. The “Press”-labeled latch on the side of the device and all buttons on the front panel (Bolus, Menu, Target, arrow keys, Set, Run/Stop) are in place and in good physical condition.
• Electronic Components: The device’s screen is active, displaying various information. The “Mains” and “Batt” lights, indicating power and battery status, are illuminated. Additionally, a red alarm/warning light (“!”) is active.
• Accessories: A transparent infusion set (IV tubing) is observed attached to the device. Apart from this, no power cable or other accessories are visible in the image.

Screen and Indicator Analysis

The following information is displayed on the device’s active screen and panel:

• Mode: “Adult” mode is selected.
• Warning: The red “!” indicator light is illuminated, and the screen displays the warning “Press RUN”. This situation is a status alert indicating that the device is awaiting a user command to start the infusion process, rather than a malfunction.
• Battery Status: The illumination of the “Mains” light indicates that the device is connected to the electrical grid, while the “Batt” light, along with the seemingly full battery icon, indicates that the battery is full and charging.
• Infusion Information:
  • SAFTI: This may be the name of the programmed setting or medication.
  • Σml: 2.6: Total fluid volume delivered.
  • Tml: 0.0: Likely the target total fluid volume.
  • dr/min: Unit representing drops per minute.
  • Σt: 00:03: Total elapsed time since the start of the process (3 seconds).
  • Tt: 00:00: Target total time.

Potential Malfunction Risk and Conclusion

Upon examination of the visuals, no critical condition such as obvious damage, cracks, dents, or cable wear that would directly affect the device’s operation has been detected. The red warning light and the “Press RUN” message are considered part of a normal operating procedure rather than a malfunction. The clean and well-maintained appearance of the device suggests it is regularly used and in good condition. No significant wear that would pose a potential malfunction risk has been observed.