Secondhand Top 3300 Infusion Pump

Objective AI Report

Disclaimer: I am Medbidding AI. I am an unbiased AI robot. I have generated the following report automatically (without human intervention). The report was prepared by examining only the product images in the ad in detail. The report may contain errors. Medbidding and other parties disclaim any liability that may arise from this report or reliance on its contents. If you have any questions or notice an error in the report, please contact Medbidding engineers.

Report date: 28.11.2025

TOP TOP-3300 Infusion Pump Analysis Report

Device Identification

The device shown in the visuals is an electronic infusion pump used for medical purposes. The device is designed in a vertical form and features a digital control panel, operation buttons, and a cover for the fluid flow mechanism. Additionally, there is an external sensor equipment (drop sensor) with a wired connection to the device.

Brand and Model

As a result of a detailed examination of the device’s front surface and bottom panel, the brand was clearly identified as TOP, and the model as TOP-3300. On the lower left corner of the front panel, the inscriptions “TOP INFUSION PUMP” and immediately below it “TOP-3300” are legible. The device’s overall design language and labeling are in full compliance with this brand/model.

Originality

The product’s casing quality, the font structure of the “Top” logo, the placement of the informational labels, and the accessory compatibility (original drop sensor slot and design) indicate that the device is an original production. The professional print quality of the warning labels on the side surface also complies with industrial standards.

Areas of Use

This device is used in hospitals, clinics, and veterinary services to precisely administer fluids, medications, or nutrient solutions intravenously to patients over a specific period and dosage. It is suitable for treatments requiring precise flow control in milliliters/hour (ml/h) instead of manual adjustment (such as chemotherapy, anesthesia, critical care medications, etc.).

Quantity Information

The visuals show 1 unit of the TOP-3300 Infusion Pump main unit and 1 Drop Sensor connected to the device with a coiled cable.

General Condition and Physical Deformations

The device is in used condition. There is a noticeable discoloration (yellowing) on the side and rear plastic casing of the product; this indicates that the device has been exposed to light for a certain period or that the plastic has undergone a natural aging process over time. However, the device’s front control panel appears whiter and cleaner compared to the side parts. There are no noticeable deep scratches, breaks, cracks, or heavy impact marks on the casing. The front panel keypad is clean, and its inscriptions are not worn off.

Mechanical and Electronic Components

Mechanically, the carrying handle located on the upper part of the device appears sturdy. The front cover latch is in place. The keypad (membrane buttons) is physically sound, and the symbols on them are clearly legible. Although the pixel status cannot be commented on as the screen is off, no breaks or cracks are visible on the screen glass.

Accessories and Connections

The integrated or external accessories provided with the device are as follows:

• Drop Sensor: There is a cream-colored sensor connected to the device with a gray coiled cable, bearing the inscription “DROP SENSOR” and an insertion diagram. No damage is observed on the sensor’s outer plastic.

Battery Status

In the upper right corner of the device’s front panel, there are LED lights under the heading “BATTERY INDICATOR”. This indicates that the device has an internal battery. However, since there are no photos of the device in operation, the battery’s current capacity, charge retention performance, or whether it has physically swelled (as it is internal) cannot be determined from the visuals.

Label Information and Technical Details

The labels on the device contain the following critical information:

• Calibration Label: On the side surface, there is a blue/turquoise label affixed by “OMKA CALIBRATION CENTER”.
  • Certificate No: 220221DA36
  • Calibration Date: 22.02.2021
  • Next Calibration Date: 22.02.2022

  This information indicates that the device last underwent a professional check in 2021, but according to the label, the next calibration date has passed.

• Error Codes Guide: On the side surface, an error code list has been affixed for user convenience:
  • AL-0: Empty container
  • AL-1: Occlusion
  • AL-2: Flow rate error
  • AL-5: Door open
  • AL-7: Air-in-line
  • Door: Door check
  • Fin: Infusion complete
  • Er: Malfunction
  • Sound only: AC power supply warning

Control Panel and Interface

The controls located on the front panel are as follows:

• Digital displays: TOTAL VOL (ml), RATE (ml/h), VOL LIMIT (ml).
• Adjustment buttons: Up/Down arrow keys, SELECT, IV SET, CLEAR, PURGE.
• Operation buttons: ON/OFF, START, STOP (with mute function).
• Status LEDs: CHARGE, Operation and Alarm indicators.

Current Fault and Risk Assessment

There is no physical evidence (broken parts, burn marks, etc.) in the visuals to suggest the device is faulty. An LED warning such as “System Error” could not be observed as the device was off. However, the fact that the calibration date on the label (2022) has passed indicates that the device requires an up-to-date technical service maintenance and calibration before use. The yellowing on the side surface is merely a cosmetic flaw and does not pose a direct risk to operational functions.