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: 11.06.2026
Report code: 1781200767
UNIKTA DA02-L Medical Examination Chair Analysis Report
Device Identification and Usage Areas
A medical examination and treatment chair has been identified in the images. This device is designed for positioning patients during various medical procedures. It is particularly suitable for use in branches such as gynecology, urology, general examination, and minor surgical interventions. The device features adjustable settings to ensure patient comfort and facilitate access for healthcare professionals.
Brand and Model Information
According to the information on the label located at the bottom of the product, the brand of the device is determined as UNIKTA and the model as DA02-L. This information clearly establishes the identity of the product.
Authenticity Assessment
The clear labels on the device, the CE mark, and the general manufacturing quality indicate that the product is authentic. The workmanship and material selection meet the expectations of a standard medical product.
Quantity Information
- Medical examination chair: 1 unit
- Wired remote control: 1 unit
- Removable armrest: 1 unit (another one is attached to the device)
- Removable footrest: 1 unit (another one is integrated into the device)
- Metal connection parts: 2 units
General Condition and Physical Deformation
The device is in a generally used condition. No significant wear, tears, or stains have been observed on the white upholstery of the chair. There are slight scratches and color fading on the cream-colored plastic components that form the main body of the device, especially on the lower parts. This indicates the usage history of the device.
Mechanical and Electronic Component Inspection
The wheels of the device appear to be sturdy, and no issues affecting its mobility have been detected. The adjustable mechanical parts visually maintain their integrity. The only visible electronic component is the remote control connected to the device via a cable. There is no physical damage or breakage found on the remote control.
Accessories and Connection Points
The device comes with one wired remote control, one removable armrest, and one removable footrest. Additionally, two metal connection parts are also present in the images. The remote control cable is connected to the device. No clear socket input or output is visible in the images.
Battery Status
No internal or external battery belonging to the device has been detected in the images. It is assumed that the device operates on mains electricity.
Label Information and Meanings
The label located at the bottom of the device contains the following information:
- Serial Number (S.N): 0916015. This number is a unique identifier for each device. It is used for production tracking, warranty processes, and service operations.
- REF Code: DA02-L. Indicates the model or reference code of the product. It is used in product identification and ordering processes.
- Production Date: 2016. Indicates the year the device was manufactured.
- Manufacturer: UNIKTA Medikal San. ve Tic. Ltd. Şti. Specifies the company that manufactured the device.
- Model: DA02-L. This is the commercial model name of the device.
- CE Mark: Indicates that the product complies with the European Union’s health, safety, and environmental protection standards.
- Made in TURKEY: Indicates that the product was manufactured in Turkey.
Screen Analysis
There is no screen on the device. Therefore, a screen analysis could not be performed.
Dimensions and Compatibility
There is no numerical information regarding the dimensions of the device or specific body compatibility in the images. However, looking at its general appearance, it is understood to be of suitable dimensions for the examination and treatment of a standard adult patient.
Production Year
The production year is clearly stated as “2016” on the label located at the bottom of the device.
Documents
No documents such as invoices, warranty certificates, or user manuals belonging to the device were encountered in the images.
Usage Duration
There is no information regarding the total usage hours or duration on the screen or labels of the device.
Existing Fault Detection
No clear evidence of a fault, such as a broken part, error message, or severed cable that would prevent the device from operating, has been detected in the images.
Potential Fault Risk
Apart from the slight scratches and color fading observed on the plastic base of the device, no concrete situation that could pose a potential fault risk, such as rusting, cable crushing, or significant wear, has been detected. The general condition of the device is good for its age.
