Secondhand AMS 200 Anesthesia Machine

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: 17.07.2025

AMS 200 Anesthesia Machine Analysis Report

Overview and Device Description

The images show a complete anesthesia machine unit mounted on a wheeled stand. The device is designed for use in operating rooms or other medical environments where surgical procedures are performed. Its primary function is to administer anesthesia by delivering a controlled mixture of anesthetic gases and oxygen to the patient and to monitor the patient’s respiratory functions. The product consists of a monitor, a breathing circuit, flowmeters, pressure gauges, and a storage area with drawers.

The total number of products shown in the images is one anesthesia machine. Various accessories are also integrated with the device.

Brand and Model Identification

The brand of the device in the image is identified as AMS from the logo located on the top-left corner of the monitor and on the wheels. The label below the monitor displays the number 200; therefore, the product model is estimated to be 200. The workmanship and logo quality give the impression that the device is an original product.

General Status and Condition

The overall condition of the device is assessed as used. While no major damage or fractures are observed in any part, there are signs of wear on moving parts such as the wheels and on the main casing due to use. The environment where the device is located is thought to be a workshop or a technical service room. The fact that the device’s screen is on indicates that it is receiving power.

Physical Deformation

Upon detailed inspection of the product’s physical condition, the following points have been identified:

• Casing: No significant cracks, fractures, or dents are visible on the main casing of the device. There may be minor scratches and color variations on the surfaces, but these are not clearly discernible.
• Drawers: The surfaces of the three white drawers on the front panel appear clean and are properly fitted in place.
• Wheels: The wheels show significant soiling and wear due to use. The “AMS” logo is present on the wheels.
• Hoses and Cables: No visible tears or crushes have been detected on the black and yellow hoses connected to the device.

Mechanical and Technical Component Inspection

The mechanical parts of the device have been visually inspected. The glass tubes of the flowmeters and their indicators appear to be intact. The dials and needles of the pressure manometers are in place. The device’s work surface and shelves appear stable. No obvious malfunction or deficiency is observed in any mechanical part.

Accessories and Connections

The images show the basic components necessary for the standard operation of the device. These include:

• The bellows and hoses that form the patient breathing circuit.
• Flowmeters for measuring gas flow.
• Manometers for indicating system pressure.
• Various gas inlet and outlet ports.

There are labels on the device indicating various systems and connection points, such as “RATIO SYSTEM (ORC)”, “OXYGEN ALARM SYSTEM”, and “AUXILIARY OUTLETS”. Apart from an external power cable, no other cables, boxes, or additional accessories are present in the images.

Screen Analysis

The screen of the device’s integrated monitor is active. A typical interface used for patient monitoring is visible on the screen. This interface displays graphical data, such as respiratory curves, and numerical parameters. No cracks, pixel errors, or abnormal images have been detected on the screen. The displayed data indicates that the device is operational and processing data, but there are no error or warning messages on the screen.

Label Information

Although the labels on the device are not clearly legible, the label below the monitor is seen to display 200. Labels containing specific production information such as serial number, REF code, or year of manufacture cannot be clearly read from the images.

Potential Risk Assessment

The overall condition of the device suggests that it is in a functional state, despite being used. No obvious risk factors requiring immediate intervention, such as rust, severe crushing of cables, or cracks in the casing, are observed in the images. Conditions like wear on the wheels are normal tear consistent with the device’s service life. However, it should be noted that this report is only a preliminary assessment based on visual analysis. As with any medical device, this product must be thoroughly inspected, calibrated, and tested by an authorized technical service before clinical use. This inspection is mandatory to detect potential malfunctions that are not visible to the naked eye.