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: 19.10.2026
Report code: 1792411439
RITMSCENAR Super Pro v.2 Transdermal Electroneurostimulator Device Analysis Report
Device Identification and Basic Information
The product in the images is a handheld therapeutic device that provides transdermal electrical nerve stimulation. The brand of the product is identified as RITMSCENAR, the model series as Super Pro v.2, and the device type as SCENAR-1-NT. The device is designed to be used in pain management and rehabilitation processes by stimulating nerve endings in the human body. The main body of the device consists of a white plastic casing, and its front surface features a color screen, control buttons, and the brand logo.
Authenticity and Manufacturing Year
Upon examination of the CE certificate, serial number, manufacturer information on the rear label, and the quality of the screen interface, it is understood that the product is original. The system startup data appearing on the device screen displays the date Mar 6 2019, while the year 2021 is printed on the rear label.
General Status and Physical Condition
The general condition of the device is new and unused. There is a protective film on the screen, and a label on this film indicates that it should be removed. There is no physical deformation such as scratches, dents, cracks, discoloration, or dirt on the casing surface.
Mechanical and Electronic Components
There are no visible mechanical issues with the outer casing, plastic parts, or the physical keypad of the device. The power button and the up/down control buttons on the front are in place. The electronic components are functioning without issues, and the color screen is actively displaying data. The device’s menu settings, treatment dose, frequency values, and battery level icon are clearly visible in the screen images.
Quantity and Accessory Inventory
The total number of products and accessories in the images has been checked, and the items included in the box have been counted individually. The images show a total of one main device, one leather carrying case, one charging adapter and cable, one original cardboard box, one user manual, and one instruction booklet. The leather carrying case is black and features a flap design without a zipper. The charging adapter’s socket input is compatible with the connection port on the side of the device.
Battery Status
The device contains an internal rechargeable battery. The charge status can be monitored via the battery icon located in the top right corner of the screen; the battery indicator is seen to be full in the screen captures. No external issues such as swelling or leakage have been observed on the battery body.
Label and Text Inventory
The text on the rear panel and the box surface has been read and listed. The rear label of the device includes the RITMSCENAR Super Pro v.2 model, the website address www.scenar.com.ru, RITM OKB ZAO manufacturer information, the CE 2265 conformity mark, EC REP representation information, serial number SN-15876, warning symbols, and a symbol to consult the user manual. The box features the text RITM OKB ZAO, Transdermal Electroneurostimulator, and SCENAR-1-NT. The protective film on the screen bears the text “Remove protective film”. These labels and codes verify the device’s place of manufacture, serial tracking, and compliance with European standards.
Screen Analysis
The device screen is a color graphic display. The startup screen displays information including RITMSCENAR Super Pro v.2, Presets 4, 0.4.2, and Mar 6 2019. The operating screens show AM, FM, and Dmp modes, an F (frequency) value of 90.7, an Int (intensity) value of 1, a Gap value of 10, and Dose 4 level settings. These data on the screen allow for the monitoring of electrical stimulation parameters applied during the treatment session.
Dimensions, Usage Duration, and Compatibility
There is no direct millimetric measurement data regarding the physical dimensions of the device in the images; however, it is understood from the images of it being held that it is of an ergonomic size suitable for handheld use. There is no counter information on the screen or labels regarding the usage duration or total operating hours.
Existing Faults and Potential Risk Status
There is no evidence of any faults such as broken parts, error messages, frayed cables, or missing components in the images. No potential risks such as severe wear, corrosion, or cable crushing have been observed, and the condition is excellent.
