Objective AI Report
Disclaimer: I am Medbidding AI. I am an unbiased AI agent. 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: 02.11.2026
Report code: 1793622737
Nihon Kohden Neurofax Electroencephalography Device Analysis Report
System Components and Device Identification
The system examined in the images consists of a Nihon Kohden Neurofax device and compatible peripherals designed to perform medical electroencephalography examinations. The setup is comprised of the main processing units positioned on a wheeled metal cart, a printer, a monitor, and a patient connection unit mounted on a separate wheeled stand.
- Brand information is read from the labels on the device as Nihon Kohden and Neurofax.
- System components include a monitor, keyboard, mouse, printer, power unit, connection box, and head lamp.
- Cable assemblies required for data input and output operations are available with the system.
Usage Areas and Purposes
This product is used in neurology clinics and sleep laboratories to record and examine electrical brain activity. It enables the monitoring of brain waves during the diagnostic process of various neurological disorders. The provided accessories and connection ports allow for the accurate transmission of signals to the device.
Quantity Information
The total number of products and parts in the images is as follows: one wheeled cart, one computer monitor on the cart, one keyboard, one mouse, one printer on the cart shelves, one LS-120 model power unit, one additional unit with a metal casing, one Neurofax connection unit on a wheeled stand to the side, and one wheeled stand with a lamp on the top.
General Status and Condition
The device and its peripherals are in generally good condition. No excessive wear or discoloration has been observed on the plastic and metal surfaces. The overall structure of the device presents a clean and orderly appearance.
Physical Deformation
There are no significant cracks, deep scratches, or dents on the casing and panels. No physical deformation has been detected on the surfaces, other than slight dust accumulation resulting from the usage environment.
Mechanical Parts
The wheels of the cart, the moving parts of the connection units, and the stand mechanisms appear to be functioning without issues. The buttons and switches are in place and appear physically robust.
Electronic Parts
The visible electronic components and connection sockets are in place. Cable connections are orderly, and no exposed broken wires or damaged insulation have been observed.
Accessories
The system includes one computer keyboard, one computer mouse, one printer, numerous signal cables, and power cables. A detailed examination of the socket inputs shows that the connection pins are in good condition. There are no consumables or accessories with an expiration date visible in the image.
Battery Status
There is no external or internal battery compartment or battery pack visible on the main units and peripherals examined in the images; the system operates directly on mains electricity.
Label and Text Inventory
The text read on the device body and panels is as follows: Nihon Kohden, Neurofax, LS-120, FLASH ENERGY 1.28J, SINGLE, POWER, SELECTOR, IMPEDANCE CHECK, PHASER 3020, PHILIPS, MICROSOFT, R, L, X1, X2, X3, X4, X5 RESP F, + BP1 -, X6 RESP C, + BP2 -, X7 RESP A, + BP3 -. These labels and inscriptions allow the user to correctly manage the channels, power switches, warnings, and connection points on the device.
Screen Analysis
The screen of the Philips-branded monitor located on the cart is turned off. No error messages or menu text are visible on the screen.
Dimensions and Compatibility
There is no direct measurement information in millimeters or inches for the products in the images. However, it is designed in dimensions compatible with standard medical device carts and clinical environments.
Year of Manufacture
There is no direct indication of a manufacturing year on the labels or documents. The design lines and the structure of the components used indicate that it belongs to a period consistent with professional medical device manufacturing standards.
Documents
There are no invoices, warranty certificates, user manuals, or any printed documents visible in the images.
Usage Duration
Since the device screen is off and there is no counter information on its labels, data regarding the usage duration or operating hours is not available in the image.
Existing Faults
In the visual inspection, there is no clear evidence of a fault such as a broken part, an error code on the screen, a broken cable, or missing essential components.
Potential Fault Risk
No concrete risks such as severe corrosion, deep cracks, or crushed cables have been observed in the images; the physical condition of the device is satisfactory.
