Secondhand Modus ED-SWT ESWT Device

Objective AI Report

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Report date: 05.01.2026

Inceler Medikal Modus ED-SWT Shockwave Therapy Device Analysis Report

Device Identification and Description

The examined images show a medical device with a touchscreen integrated onto a wheeled stand. The product is a system consisting of a main control unit, a trolley stand, an application head (applicator), and connecting cables. Labels on the device and the screen interface prove that it is an ESWT (Extracorporeal Shockwave Therapy) device.

Brand and Model Information

All logos on the images, front panel inscriptions, and the rear type label have been examined in detail, and the product’s brand and model information has been definitively identified.

• Brand: Inceler Medikal (INCELER MEDIKAL LTD. ŞTİ.)
• Model: Modus ED-SWT

The model name is clearly visible in capital letters on both the front panel and the side body of the device. The rear label confirms that the manufacturer is “İnceler Medikal Sağlık Hiz. San. Tic. Ltd. Şti.” and that the product is domestically manufactured with the inscription “Made in TR – TÜRKİYE”.

Originality and Production Year

Upon examining the labeling standards, CE (1984) marking, logo print quality, and software interface details on the product, it is observed that the product is completely original. The rear label of the device clearly states “ÜRETİM YILI (PRODUCTION YEAR): 2022”. This indicates that the device is relatively new, approximately 3-4 years old (as of the report date).

Areas of Use

This device is an ESWT system that provides therapy using extracorporeal shockwaves. Considering the “ED” abbreviation in the model name and its equivalent in medical literature, it is understood that the device is specifically designed for the treatment of Erectile Dysfunction (Impotence). However, due to general ESWT principles, it also possesses the technical infrastructure to be used for shockwave therapy (pain management, tissue healing, etc.) in orthopedic and physical therapy fields. It is a professional device suitable for hospitals, clinics, and urology polyclinics.

Label and Technical Data

The technical data read from the metal label (Image 4) located on the back of the device is listed below:

• Serial No: IMED-850-2261
• Device Type: Extracorporeal Shockwave Therapy Device
• Voltage / Current: 220-240 V / Max. 2 A
• Frequency: 50 – 60 Hz
• Power Consumption: 50 VA
• Maximum Pressure: 10 BAR
• Protection Class: IP20 / Class IIb / Type B
• Standard: IEC 60601-1 (Class 1 Type B)

Usage Duration and Screen Analysis

The device is in working condition, and the counter information on its touchscreen has been analyzed in detail via the second image. This data provides precise information about how intensively the device has been used:

• Device Number (Software): 770926
• Focus Generator Count: 2,061,700 (Considered to be the total number of shots).
• Focus Applicator Shot Count: 40,150 (This is the usage count of the current applicator).

The device’s total generator counter is over 2 million, but the currently installed applicator has made approximately 40 thousand shots. The “Reset Applicator Count” button appears active, indicating that the counter is reset during applicator replacements or maintenance. The screen brightness and readability are in very good condition.

Physical Condition and Deformation Analysis

Based on the data obtained from the images, the physical condition of the device is as follows:

• Outer Casing: The device’s white metal/plastic body is generally clean. No major visible scratches, cracks, or dents have been detected. The “modus ED-SWT” inscriptions are unfaded and clear.
• Mechanical Components: The wheels of the stand (Image 1) appear sturdy. There is no visible damage to the handle or mechanism of the drawer located at the front.
• Applicator (Head) Condition: Image 3 shows the inner part of the hand probe. Although there are slight blackenings/marks on the metal teeth due to use, the structure of the teeth appears intact. There is no indication of the applicator having sustained impact (dent, broken plastic).

Accessories and Cables

The components displayed with the system are as follows:

• 1 Main unit and integrated touchscreen.
• 1 Original trolley stand (with drawer).
• 1 Hand applicator (probe) and spiral connection cable.

No bending or risk of breakage has been observed at the socket points where the applicator cable connects to the device, but the form of the grey spiral protector may have gained flexibility due to use.

Current Malfunctions and Potential Risks

Since the device’s screen is working and displaying the menu without error codes (Image 2), it can be said to be electronically functional. No red alarm regarding a “Focus Generator” warning or malfunction is visible on the screen. Only the slight wear on the inner part of the applicator in Image 3 indicates that this component (electrode/applicator interior) is a consumable item and may require periodic replacement. There is no rust, liquid contact traces, or severe impact damage in the general structure of the device that would cause concern to the buyer.

Quantity Information

The images show only 1 (one) unit of the main device and its associated components (stand and applicator).

General Condition Assessment

The Inceler Medikal Modus ED-SWT device, being a 2022 production, is a second-hand medical device with modern technology, cosmetically very clean (8.5/10), and with functional electronics. Despite having a total shot count of over 2 million, it appears well-maintained, and the current applicator’s condition is active. Based on visual analysis, it is assessed as being directly ready for use in a clinical setting.