Secondhand Anesthesia Machine Draeger Fabius

Objective AI Report

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Report date: 19.11.2025

Dräger Fabius Anesthesia Machine Analysis Report

Device Identification, Brand, and Model Determination

As a result of detailed examination of the visuals, the product has been identified as a medical anesthesia workstation. On the device’s front panel, in the upper left corner, the Dräger brand logo is clearly and legibly visible. On the right side of the front panel, the product’s model is stated as Fabius. In light of this visual data, the device’s brand and model have been definitively confirmed as Dräger Fabius. The product is an anesthesia machine equipped with manual flow tubes (flowmeters) and an electronic ventilator control unit.

Areas of Use and Function

This device is designed to administer general anesthesia to patients in hospital operating room environments, support respiration, and precisely adjust and deliver gas mixtures (Oxygen, Nitrous Oxide, Air) to the patient. The device in the visuals is the main unit and plays a central role in the anesthetic management of a medical operation.

General Condition and Originality Assessment

Considering its design, color palette (Dräger’s typical light gray and blue tones), material quality, logo placement, and industrial craftsmanship, the product is an Original Dräger manufactured device. Upon examining its general condition, it is understood that the device is used, but in a well-preserved state. It is in the condition of a second-hand medical device from a hospital environment.

Physical and Mechanical Examination

• Casing and Body: There are no visible major dents, cracks, or significant signs of rust on the device’s metal casing. The panel joints are smooth.
• Control Panel: The button sets of the electronic control panel on the upper part appear complete. No severe wear is visible on the gelatin or coating of the panel.
• Drawers and Shelves: The lower part of the device features two large white storage drawers, and above them, a blue/purple colored fold-out work surface/shelf. These sections appear visually sturdy.
• Wheel System: The wheels that enable the device’s mobility are present, and orange/yellow protective bumpers are visible on the base. No significant breakage has been detected in the wheel structure.
• Flowmeters: The glass tubes of the flowmeter unit located on the front right are intact. Three black control knobs are present beneath them.
• Vaporizer Unit: In the front-center part of the device, there is a railed area (manifold) designated for vaporizer (evaporator) attachment. However, this area with the locking mechanisms is empty; no vaporizer is attached.

Rear Panel and Connection Analysis

In the visuals of the device’s rear section, medical gas inlet blocks (manifold) and tube securing areas are visible:

• Gas Cylinder Holders: In the rear lower body, there are recessed areas for placing two medical gas cylinders and black straps used to secure these cylinders. The straps appear sturdy.
• Inlet Ports: On the rear left side, multiple gas inlet sockets (pipeline inlets) are vertically arranged. The covers or connection points for these sockets are present in the visual.
• Cabling: A black power cable is wrapped around the device. Visually, no crushing or breakage has been detected in the cable.

Label and Technical Information Review

Technical labels are located on the rear panel and sides of the device:

• Product Label: On the rear upper right panel, there is a white technical information label, including the CE mark. However, due to the visual resolution, the serial number (SN), year of manufacture, or REF code on this label are not clearly legible.
• Yellow Warning Labels: Small yellow labels resembling periodic maintenance or safety warnings are visible on the rear section.

Missing Parts and Accessories

The product in the visuals is not a “plug-and-play” set ready for operation; some main components are not present in the visuals:

• Vaporizers: The vaporizer units (typically Sevo/Iso) where the anesthetic gas is vaporized are not attached to the device; their slots are empty.
• Breathing Circuit: Patient hoses, breathing bag, and CO2 absorbent canister are not present in the visuals. Although a mounting point for the breathing circuit arm is visible on the left side, the arm itself is not attached.
• Monitoring Screen: Some Fabius configurations include an external patient monitor; in this visual, no external monitor is present, only the device’s own internal LCD control screen.

Potential Malfunction Risk and Warnings

There is no concrete evidence in the visuals indicating that the device is “FAULTY” (e.g., broken screen, severed cable, error message). However:

• Since the device contains sensitive pneumatic and electronic systems, the condition of the gas flow sensors and battery (internal backup battery) cannot be visually confirmed.
• Although the gas inlet seals and hose connection points on the rear appear visually clean, their sealing integrity can only be determined through technical testing.
• In its current state, the device can be reported as being in “good physical condition” and having “preserved integrity.”