Defective Secondhand Medonic M20S BD ABR Hemogram Device

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: 22.11.2025

Medonic Hematology Analyzer Device Detailed Analysis Report

Device Identification

The examined visuals belong to a professional, desktop-type hematology analyzer device used for blood testing and counting (Complete Blood Count / CBC) procedures in medical laboratory environments. The device’s general design structure, sample inlet channels, and control mechanisms confirm this identification.

Brand and Model

In the visuals, the Medonic brand logo and name are clearly visible on the lower part of the device’s front panel. However, an alphanumeric designation (e.g., M-Series, CA530, M32) that would definitively identify its model was not found to be 100% legible on the product images, either on the device body or its labels. Therefore, while the brand is certainly Medonic, the model information has not been specified in the report. The device’s general casing structure suggests older generation series of the brand.

Originality

The font of the “Medonic” print on the front face of the device, the design of the plastic mold, the unique sampling latches used, and the print quality of professional technical terms like “Start 1:1” / “Start 1:200” indicate that the product is an original Medonic production.

Areas of Use

This device is used in clinics and hospital laboratory departments for analyzing blood samples taken from patients (counting leukocytes, erythrocytes, thrombocytes, etc.). The “Start 1:1” and “Start 1:200” indications on the front panel show that the device can perform sampling in both whole blood (undiluted) and prediluted (diluted – typically for capillary blood) modes.

General Condition

The general condition of the device appears to be at a level requiring maintenance or repair and in “scrap/spare parts” status. The integrity of the device is compromised, its most critical component, the display module, has been removed, and the internal components are exposed. The product is far from appearing as a functional device.

Physical Deformation

• Front Panel: The most prominent deformation is in the area where the screen should be. The screen glass, LCD panel, and its frame have been completely removed; the electronic circuit board (PCB) is directly visible.
• Contamination: Heavy accumulation of dust and dirt is present on the surfaces of the device’s plastic casing, between the buttons, and in the ventilation channels.
• Scratches: Friction marks and stains are observed on the beige-colored surfaces of the casing, attributed to usage and storage conditions.

Electronic Components and Screen Analysis

The device does not have a screen. In the visual, a green printed circuit board (PCB) is present where the screen should be. The following details have been identified on this board:

• The technical print “sinact 94V-0” is present on the PCB.
• The codes “D4555-02” and “DB1113157” are legible on the circuit board.
• Various chips and data pathways are visible to the naked eye on the board; there is no protective cover.

The removal of the screen indicates that the condition of the electronic components is uncertain and represents a potentially serious deficiency.

Mechanical Components

• Sample Inlets: Two sample inlet compartments (with a mechanical paddle/pedal structure) are located at the bottom of the front panel. On the left-hand pedal, a white, hard foam or plastic-like piece appears to be jammed.
• Lateral Mechanism (Rotary Wheel): On the left side of the device, there is a large blue gear wheel system (thought to be a type of automatic sampler or reagent mixing disc). This wheel has white, circular slots. The red cables at the connection points between the wheel mechanism and the device body are exposed and appear disarrayed.

Accessories and Missing Parts

• A blue rotary disk accessory, integrated into or subsequently attached to the left side of the device, is present.
• Missing: Power cable, display module, display frame, and probable external casing screws are missing.
• No reagent (solution) containers or connecting hoses are visible in the visuals at the back or side of the device.

Label and Technical Information

The legible technical terms on the device are as follows:

• Brand: Medonic
• Sampling Modes: “Start 1:1” (Direct Sample), “Start 1:200” (Diluted Sample)
• PCB Codes: DB1113157, D4555-02, sinact 94V-0 (These codes belong to the device’s motherboard or control board).

Quantity Information

A total of 1 main device body was analyzed in the visuals. The blue disc on the left side was considered a connected part of the device.

Potential Failure Risk

Due to the missing display panel and exposed circuit board, the product is in a “UNUSABLE” state. Direct exposure of internal circuit components to moisture, dust, and static electricity significantly increases the risk of permanent damage to the device’s electronic boards. Furthermore, the loose cables of the mechanical unit on the left side indicate a broken electromechanical connection. In its current condition, the device appears suitable only for sourcing spare parts (casing, mechanical parts, etc.).