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: 15.07.2026
Report code: 1784105746
OpStar MI 20 Infusion Pump Analysis Report
Device Identification and Brand Model Information
One infusion pump has been identified in the images. The “OpStar” brand and the phrase “Infusion pump” are clearly legible on the label located on the front of the device. Additionally, the model code “MI 20” is specified in the upper right part of the label. This device is a medical instrument used in hospitals or home care settings to deliver fluids (medication, nutrients, etc.) to patients at a specific rate and volume.
Authenticity Assessment
Upon examining the logo quality, the clarity of the labels, and the general workmanship details on the device, the impression is that the product is original. No signs of counterfeiting or low-quality production details have been observed.
Usage Areas
The OpStar MI 20 infusion pump is used to deliver medications, nutritional solutions, or other fluids into a patient’s body in a controlled manner at a specific flow rate and volume. Such devices are generally preferred in various medical specialties, including intensive care units, operating rooms, emergency services, oncology units, and home care services, for intravenous or enteral (via feeding tube) applications.
Quantity Information
The main product analyzed in the images is one OpStar MI 20 infusion pump. No additional accessories or spare parts are present in the images along with the device.
General Condition and Physical Deformation
The general condition of the device is considered used. There are no significant dents or cracks on the casing. However, there are multiple scratches on the screen surface. No significant fading in the device’s color or heavy dirt/dust accumulation has been observed.
Mechanical and Electronic Component Inspection
No visible issues have been detected in the mechanical components of the device, particularly in the roller mechanism on the right side where the infusion set is placed. The physical integrity of the buttons on the control panel, such as “Start/Stop”, “+”, “-“, directional keys, “OK”, “Mode”, “BOL”, and “C”, has been maintained. As for the electronic components, the screen does not present an active display because the device is turned off. The fact that the screen is off prevents a visual assessment of its electronic functionality.
Accessories and Socket Inputs
There are no external boxes, cables, or other accessories belonging to the device in the images. To the left of the device’s screen, there are icons representing socket inputs in the form of a power plug and a battery symbol. These icons indicate that the device can be connected to an external power source and possesses an internal battery.
Battery Status
There is a battery symbol on the left side of the device’s screen. This symbol indicates that the device has an internal battery. However, there is no information or indication in the images regarding the current charge level, capacity, or physical condition (such as swelling or leakage) of the battery.
Label Information
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- Brand: OpStar
OpStar is the manufacturer brand of the infusion pump. This information specifies the identity and origin of the device.
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- Model: MI 20
MI 20 refers to the specific model of the device. This code is used to determine the technical specifications and compatibility of the product.
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- Product Type: Infusion pump
This phrase explains the primary function of the device, meaning it is designed to perform fluid infusion.
Screen Analysis
The device’s screen is in the off state and does not display any text, warnings, menus, or values. There are visible scratches on the screen surface. These scratches affect the visual integrity of the screen.
Dimensions and Compatibility
There is no direct information in the images regarding the specific dimensions of the device or user compatibility. However, infusion pumps are generally designed in sizes that can be mounted on standard IV poles or bed rails. The general structure of the device suggests that it is of a size suitable for portable use and use in clinical environments.
Year of Manufacture
There is no label or document information regarding the year of manufacture of the device in the images. The general design and physical condition of the device have an appearance similar to modern medical devices, giving the impression that it may have been produced in recent years. However, it is not possible to specify an exact year of manufacture.
Documents
There are no invoices, warranty certificates, user manuals, or other documents belonging to the device in the images. Therefore, it is not possible to provide information based on visual evidence regarding the warranty status or usage details of the device.
Usage Duration
No information regarding the total usage hours or duration of use has been detected on the device’s screen, labels, or any documents in the images. This data could have been an important indicator of the device’s past performance, but it cannot be determined through visual evidence.
Existing Faults
There is no clear evidence of a fault in the images, such as a broken part, error message, or severed cable that would prevent the device from operating. The scratches on the device’s screen are a physical deformation and have not been evaluated as a direct functional fault.
Potential Fault Risk
The general condition of the device is good. No serious wear or rusting has been observed on the casing. Apart from the scratches on the screen, there are no concrete visual clues indicating a potential risk of failure.
