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: 30.09.2026
Report code: 1790772981
CLASSYS ULTRAFORMER III Device Analysis Report
Device Identification and Basic Information
The analyzed device is a system featuring focused ultrasound technology used in medical and aesthetic applications. The main body of the device is designed in white and is mounted on a wheeled base that provides mobility. The system features an adjustable screen at the top and carries two application handpieces integrated into the body. According to the information on the technical label, the brand of the device is determined as CLASSYS and the model as ULTRAFORMER III.
Areas of Use
This device is used to perform aesthetic and dermatological procedures such as skin tightening, face lifting, and body contouring by using focused ultrasound waves. It is preferred in medical aesthetic clinics to improve skin quality and support tissue regeneration processes. The handpieces located on the device offer the ability to perform treatments by focusing on skin layers at different depths.
Quantity Information
In the examination of the images, there is 1 main console device, 2 application handpieces connected to the console, 2 cartridges attached to the handpieces, and 4 wheels that move the device. The total count of parts and the main unit is completed in this manner.
General Status and Condition
The device is generally clean and in good condition. No yellowing or discoloration has been observed on its plastic outer casing. The exterior surface of the system, which appears to have been used in a clinical environment, looks well-maintained.
Physical Deformation
There are no cracks, deep scratches, or dents on the outer casing, screen frame, or wheel sections of the device. No clear deformation has been detected on the surface, other than slight dust residues depending on usage conditions.
Mechanical Components
The wheels, handpiece slots, mechanical locking mechanisms, and the screen support arm move smoothly. It is observed that the handpieces fit perfectly into their slots on the body. There is no physical breakage or fracture at the ventilation grilles and cable exit points.
Electronic Components
The electrical cable input socket and power connection points are located at the lower rear part of the device. Connection ports are located on the rear panel of the screen. Since the screen is in the off position in the images, the electronic interface could not be tested, but the pin structure of the socket inputs is intact.
Accessories and Connection Ports
Accessories included with the device are two gray-colored application handpieces and cartridges attached to the tips of these handpieces. A green-labeled cartridge with the code L7-3.0 is attached to the tip of one of the handpieces, and a blue-labeled cartridge with the code L4-4.5 is attached to the tip of the other. The power cable and screen data connection sockets are located on the rear panel of the device.
Battery Status
There is no internal or external battery in the device; the system operates directly on mains electricity.
Label and Text Inventory
The texts read on the technical label on the rear panel of the device and on the body are as follows: In the upper section, there are the barcode and the codes (01)08800016900026, (11)221222, (21)CUR22L062. The main label reads Focused Ultrasound Therapeutic Equipment, ULTRAFORMER III, Model: UF3-M300, Rating: 100-240V~, 50/60Hz, 500VA, Weight: 35kg. The serial number is stated as SN CUR22L062 and the production date as 22.12.22. Additionally, there is the CE 0068 mark, warning symbols indicating that the user manual should be read, Classys Inc. as manufacturer information, and the Made in Korea text indicating that it is produced in South Korea. Information for the European representative MT Promedt Consulting GmbH and German address details are available. The ULTRAFORMER III series text is on the body, and the CLASSYS logo along with L7-3.0 and L4-4.5 cartridge size information are on the handpieces. This label data informs the buyer of the device’s electrical requirements, compliance standards, and traceability number.
Screen Analysis
The CLASSYS logo is visible on the frame of the screen located at the top of the device. Since the screen is in the off position, interface menus, warning messages, or operating values are not visible in the image.
Dimensions and Compatibility
It is stated on the technical label that the weight of the device is 35kg. The wheeled structure of the device allows it to be portable within the clinic. The handpieces and cartridges are designed to work only with compatible equipment in this series.
Year of Production
The production date is clearly written as 22.12.22 on the technical label on the rear panel of the device. This information indicates that the device was produced in December 2022.
Documents
There are no invoices, warranty certificates, user manuals, or any printed documents in the images.
Usage Duration
Due to the screen being off and the absence of an operating hour counter on the labels, there is no data in the image regarding the total usage time or shot count of the device.
Existing Faults
There is no evidence of any fault such as broken parts, severed cables, liquid leakage, or error messages in the images.
Potential Fault Risk
The external condition of the device is very good; the cables are not crushed, and no rusting or deep wear has been observed on the casing. Based on visual evidence, no risk of a fault occurring in the near future is foreseen.
