Secondhand Elekta Linac Linear Accelerator

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: 18.09.2025

Elekta Precise Linear Accelerator System Analysis Report

Device Description and Intended Use

The images show a linear accelerator (LINAC) system used for radiotherapy (radiation therapy) in oncology, along with its disassembled parts. The device is an advanced medical system used in cancer treatment. While the first two images show the device in an installed and operational state, the other images indicate that the system has been disassembled and stored on pallets. The report is based on visual evidence of both the installed and disassembled states of the device.

Brand and Model Identification

Upon detailed examination, the device’s brand was identified as Elekta, and its model as a treatment system belonging to the Precise series. This information was confirmed by the clearly legible phrase “ELEKTA LIMITED” on a label on a disassembled electronic component and the text “Precise Treatment System” written on the device’s main body (gantry). A “radon” brand logo is present on the patient table, which may indicate that the table or its mattress belongs to a different manufacturer.

General Condition and Assessment

The device is in a used and disassembled state. The first images show the system installed in a healthcare facility with its screens on, meaning it was powered and operational. This suggests that the device was functional before disassembly. Subsequent images show that the main components (gantry, electronic cabinets, etc.) have been disassembled, wrapped in stretch film, secured on wooden pallets, and moved to storage. Although the parts appear generally neatly disassembled, there is dust and dirt on them due to the storage environment. No serious physical damage or breakage is immediately apparent.

• Originality: The device’s general structure, component quality, and the logos and inscriptions on it indicate that the product is an original Elekta system.
• Quantity Information: The images show the parts of 1 complete linear accelerator system. These parts include the main gantry unit, electronic control cabinets, various power and signal modules, and one HP brand computer case.

Physical and Technical Assessment

The device’s parts, both in their installed and disassembled states, have been visually inspected.

• Physical Deformation: No significant dents, cracks, or rust have been observed on the casings or metal surfaces of the disassembled parts. Only superficial scratches and dirt, which may have occurred during the transportation and storage process, are present.
• Mechanical Components: The mechanical condition of the gantry and patient table, which are the movable parts of the device, cannot be fully assessed due to their disassembled state. However, no mechanical breakage or disintegration is visible in the images.
• Electronic Components: The internal parts of the disassembled electronic cabinets and modules are visible in the images. Wiring and circuit boards are in place. No obvious burn marks or leakage traces were found on the components. The HP brand computer case, which is part of the device’s control system, is tied with a rope to a cabinet.
• Accessories: The main components of the system are present in the images. However, it is not clear whether interconnecting cables, software, and other small accessories are complete.

Label and Screen Information

Upon examining the labels and screens in the images, the following details were identified.

• Label Information: No clearly legible serial number, REF code, or lot number was identified on the labels of the parts. An “ELEKTA LIMITED” manufacturer label is present on an electronic module.
• Screen Analysis: In the photos where the device is installed, the control screens are visible as open and active. The screens display parameters and numerical values showing the device’s position information, such as “Gantry”, “Coll”, and “Couch”. This confirms that the device was functionally operational via software before disassembly.

Potential Risk Assessment

The images do not show any direct fault logs or error messages related to the device. The biggest risk associated with the device stems from its disassembled state. During the disassembly, transport, and storage of such complex medical systems, there is a risk of damage to sensitive electronic or mechanical components. For the system to be brought back into operational condition, it must be professionally installed and calibrated by a competent technical team, and all parts must be complete and undamaged. As the functionality of any part cannot be tested in its current state, there are risks of unexpected failures after installation.