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: 27.08.2026
Report code: 1787841614
Modus ED-SWT Shock Wave Therapy Device Analysis Report
Device Identification and Credentials
The device in the image is a shock wave therapy system used for therapeutic purposes in the field of urology. The brand and model of the product are identified as modus ED-SWT based on the inscriptions on the device body and display panel. The manufacturer’s logo and the inscription Inceler medikal ltd. are located on the top right corner of the device panel. Upon examining the unique design details, label placement, and logo print quality of the device in the image, it is understood to be original.
Usage Areas and Functionality
This device is designed for extracorporeal shock wave therapy (ESWT) applications, which generate low-intensity acoustic sound waves and focus them on the targeted area of the body. Its primary area of use in the urology branch is the treatment of conditions such as vasculogenic erectile dysfunction, Peyronie’s disease, and chronic prostatitis. During the treatment process, it aims to increase blood circulation and support tissue regeneration by triggering the formation of new blood vessels (neovascularization) in the target area.
Quantity Information and General Condition
The image shows one treatment head (applicator) connected to the main body and one control and main unit console. The device appears clean and in good condition overall; it possesses the physical integrity suitable for use in a clinical environment.
Physical Deformation and Mechanical Components
There are no fractures, deep cracks, dents, or discoloration on the white plastic and metallic parts forming the main body of the device, the screen frame, or the front drawer compartment. The handle of the front cover drawer, which is considered a mechanical component, is in place and fits perfectly into the casing. The black-colored treatment head positioned on the right side of the device and the flexible connection cable carrying the head stand firmly without any bending or crushing.
Electronic Components and Screen Analysis
The integrated electronic screen on the front of the device is active. On the screen interface, ESWT and Shockwave Therapy are written in white letters on a blue background. In the middle left part of the screen, the inscription Enter Password: is visible, along with a password entry field and a numeric keypad (numbers 1 through 9, delete, and arrow keys) below it. This screen interface indicates that a security password entry is expected to prevent unauthorized use of the device. No error codes, pixel loss, or burn marks are visible on the electronic circuits or the screen glass of the device.
Accessories and Battery Status
There is one shock wave therapy head with a black and white color combination integrated into the main unit in the image. No battery compartment, charging indicator, or portable power supply label was found in the image regarding an external or internal battery for the device; it is understood that the system operates directly on mains electricity.
Label and Inscription Inventory
The texts read throughout the image are as follows: Inceler medikal ltd. logo on the top right corner of the top panel, ESWT Shockwave Therapy on the top left corner of the screen, Enter Password: on the screen entry line, numeric keys along with DELETE and OK inscriptions on the numeric keypad, modus ED-SWT model on the right side of the screen, and the modus ED-SWT brand and model inscription in a vertical position on the lower front part of the main body. These inscriptions verify the identity, manufacturer, and active operating menu of the device.
Dimensions, Compatibility, and Year of Manufacture
There is no technical label in the images indicating the exact dimensions or weight of the device. Considering the type of product and its position on the surface, it is of standard medical console dimensions. There is no clear year or date of manufacture visible on the device labels; however, given its modern industrial design, digital screen technology, and outer casing form, it can be said to belong to a current production period.
Documents and Usage Duration
There are no printed documents such as invoices, warranty certificates, user manuals, or similar items in the images. No counter information indicating the total operating hours (device lifespan or number of sessions) is readable on the screen or outer surface of the device.
Existing Faults and Potential Risk of Failure
There is no clear evidence of a fault in the images, such as broken parts, error messages on the screen, severed cables, or missing components that would prevent the device from operating. Visual inspection shows that the cables are not crushed and the body does not exhibit rusting or excessive wear, and its general condition is solid and in good state.
