Objective AI Report
Disclaimer: I am Medbidding AI. I am an unbiased AI agent. 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: 30.10.2026
Report code: 1793368901
Fotona SP Dynamis Medical Laser System Analysis Report
Device Identification and Basic Information
The device in the provided images is a professional medical laser system designed for aesthetic and surgical applications. The device features a main body, mobile transport wheels, an articulated guiding arm positioned on the top, and a touch control screen on the front surface.
- Brand and Model: Fotona SP Dynamis
- Authenticity: The brand logos, screen interface, and warning labels on the device comply with original manufacturer standards.
- Quantity Information: The images show 1 main laser device and 1 foot pedal connected to the device.
- Usage Areas: It is used in branches such as dermatology, aesthetic surgery, dentistry, and gynecology for skin resurfacing, hair removal, vascular treatments, and surgical incision procedures.
Condition, Physical and Mechanical Status
The outer casing of the device consists of white plastic and metal panels. Its general condition is clean and in good state.
- General Condition: The device is in used condition, but there are no signs of deformation on its outer surfaces and panels.
- Physical Deformation: There are no deep scratches, dents, cracks, color fading, or dirt layers on the body.
- Mechanical Components: The articulated arm system that transmits the laser beam, wheels, ventilation grilles, and the key mechanism on the front panel appear to be in good working order.
- Electronic Components: The touch screen on the front is active; the cooling fans and port inputs on the rear panel are clean.
- Accessories: The power cable integrated into the device is wrapped on the rear panel, and there is 1 gray foot pedal on the floor.
- Battery Status: No internal or external battery unit is shown in the images; the device operates on mains electricity.
Label, Text Inventory and Technical Data
There are various labels and texts on the body surfaces, rear panel, and screen of the device. The readable texts are as follows:
- The Fotona and Fotona lasers brand names are present on the front and rear panels, with the SP Dynamis model name at the bottom.
- On the technical label on the rear panel, the voltage value is stated as 220-240 V, frequency as 50/60 Hz, and current value as 16 A.
- The maximum weight limit of 135 kg is stated on the rear label.
- The side panels and warning labels contain the safety warning: CAUTION – CLASS 4 VISIBLE AND INVISIBLE LASER RADIATION WHEN OPEN. AVOID EYE OR SKIN EXPOSURE TO DIRECT OR SCATTERED RADIATION; this warning indicates that the device contains class 4 laser radiation that requires avoiding eye and skin contact when opened or due to reflections.
- In the screen interface, under the Counter menu heading, the total Er:YAG pulse count is listed as 2770127 and the total Nd:YAG pulse count as 9667291; these values indicate how long the device’s respective laser sources have been in operation.
Screen and Operating Time Analysis
The color touch screen on the front of the device is actively working. The counter menu is open on the screen.
- Screen Analysis: Usage counters for the Er:YAG and Nd:YAG laser modules are clearly readable on the screen interface.
- Usage Time: There is no direct hour information regarding how long the device has been powered on, but the total pulse counters clearly reveal the device’s historical usage volume.
Dimensions, Year of Manufacture and Documents
There is no direct text indicating millimetric measurements regarding the physical dimensions of the device, but the 135 kg weight information stated on the rear label is a critical limit for the transport and placement of the device.
- Year of Manufacture: There is no concrete date of manufacture printed on the rear label; however, when the device’s design language and screen technology are evaluated periodically, it is understood that it belongs to a modern production period with professional medical standards.
- Documents: No invoice, warranty certificate, or printed user manual is included in the images.
Fault and Risk Assessment
The visual inspection performed on the device reveals no issues that would hinder its functionality.
- Current Fault: No broken parts, error messages, severed cables, or missing components were detected in the visual evidence.
- Potential Fault Risk: No serious wear, rust, or cable crushing was observed on the casing; the condition of the device is good.
