Secondhand GE Logiq 200 Pro Ultrasound Machine

Objective AI Report

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Report date: 09.01.2026

GE LOGIQ 200 PRO Series Ultrasound Device Analysis Report

Device Identification

The device examined in the images is a mobile ultrasound system with a wheeled stand, used for medical diagnosis and imaging purposes. The system consists of a main console (monitor and control panel), probe connection ports, accessory holders, and an integrated trolley. Additionally, a probe (transducer) is visible next to the system.

Brand and Model

As a result of detailed visual inspection, the brand and model of the device have been definitively identified:

• Brand: GE (General Electric)
• Model: LOGIQ 200 PRO Series

This identification is based on the inscriptions “LOGIQ 200” and “PRO Series” located in the upper left corner of the device’s monitor frame, as well as the large “GE” logo clearly visible on the side body of the device and the “PRO Series” text below it. The product is a classic model with black-and-white imaging technology and a CRT monitor.

Authenticity

Upon examining the product’s body design, GE-specific logo placements, keypad layout, interface software, and label fonts, the product has been assessed as completely original. No signs of third-party modifications or assembled parts were found.

Areas of Use

This device is used for radiological diagnosis in medical imaging centers, hospitals, and private clinics. As understood from the software on the screen, the device is specifically configured for use in Obstetrics and Gynecology. It is also suitable for general abdominal, urology, and superficial tissue imaging. It provides black and white (B-Mode) ultrasonography services.

Quantity Information

In total, the images show 1 unit of the main ultrasound device and 1 unit of an ultrasound probe (transducer) seen attached to/held by the device.

General Condition

The device is in a used and actively operated condition. Technologically, it belongs to an older generation (CRT monitor era). The general condition of the device is “medium”; it is understood from the screen display that it is operational, but it shows significant cosmetic signs of aging.

Physical Deformities

• Color Change (Yellowing): There is noticeable yellowing (oxidation) on the device’s control panel keypads (especially around the QWERTY keyboard section and trackball) and plastic probe holders, caused by time and light exposure.
• Casing: The device’s side panels and monitor casing are intact; no major cracks or fractures have been observed. However, there are dirt and surface stains resulting from use.
• Probe: In the close-up probe image (Image 3), it is seen that the plastic body of the probe has yellowed, there is accumulated dirt from use at the joints, but the acoustic lens (gray surface) part is clean and smooth.

Mechanical Components

The device is seen standing on its wheels, and its trolley appears sturdy. The rotary knobs, TGC (Time Gain Compensation) sliders (8 units), and trackball (cursor ball) on the control panel are physically in place. The carrying handle located on the side appears sturdy.

Electronic Components

The device’s most important electronic indicator, the monitor, is operational. The screen clearly displays the classic blue phosphor ultrasound interface. Screen brightness and contrast appear sufficient for the readability of the texts on it. Due to its CRT technology, the back of the screen has a convex structure.

Accessories

• Probes: At least one probe is visible on the device. Upon close-up examination in Image 3, the tip of the probe appears flat (resembling a linear array). However, since the general intended use of the ultrasound appears to be obstetric, it might also be used with convex probes. No externally visible cuts or breaks have been detected in the probe’s cable.
• Cables: Monitor and probe cables are present on the device.
• Gel Holder: On the right side of the console, there is a transparent container/slot for placing ultrasound gel.

Battery Status

This type of device (LOGIQ 200 series) typically operates directly with mains electricity (AC power) and does not offer mobile use with an internal battery (only a memory/BIOS battery might be present). Therefore, the device must be used plugged into an outlet.

Screen Analysis and Data

Upon detailed examination of the device’s active screen, the following information can be read:

• User Information: The text “OP.DR. ESRA BOYBEK” is clearly visible. This indicates that the device belongs to or is identified by a specialist doctor.
• Date: The date “14/11/23” is located in the upper right corner of the screen. This indicates that the device was operational on November 14, 2023, and its clock was kept current (or recently current).
• Measurement Parameters: The menu contains abbreviations such as “BPD” (Biparietal Diameter), “HC” (Head Circumference), “AC” (Abdominal Circumference), “FL” (Femur Length), “CRL” (Crown-Rump Length), and “GS” (Gestational Sac). These technical terms prove that the device is in ready mode for pregnancy monitoring (obstetric measurements).

Dimensions and Compatibility

The device is designed to stand on the floor in clinical settings (cart-based system). It is much larger than portable laptop-type ultrasounds and requires a fixed space. It is compatible for adult, pediatric, and obstetric imaging as long as the appropriate probe is attached.

Documents

No printed user manual, warranty certificate, or invoice belonging to the device is found in the images.

Current Malfunctions

No critical error message such as “System Error” or physically broken/fragmented components are seen in the images. The device is awaiting operation in “Measurement” mode. However, the yellowing of the device’s buttons may indicate dust accumulation under the keypads or reduced button sensitivity.

Potential Malfunction Risk

Considering the age of the product and the yellowing of its plastic components, there might be age-related fatigue in its electronic boards or the CRT monitor tube. Especially old-style trackball mechanisms can accumulate dust over time and become stiff. Keypad contact problems may occur. However, no immediate risk factor (liquid contact trace, burn, heavy impact) that would prevent its current operation has been visually identified.