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: 31.08.2026
Report code: 1788161341
GLOBUS DUO TENS Device Technical Analysis Report
Device Identification and Basic Information
The product examined in the images is an electrostimulator device used in the medical and physical therapy field. According to the markings on the front and the rear label of the device, the brand is identified as GLOBUS and the model as DUO TENS. The rear technical label contains the following information: Electrostimulator Type: A3R, Model: DK7-065-0200-EU, and DOMINO s.r.l. – Via Vittorio Veneto, 32 31013 Codognè (TV) – IT.
Authenticity and Condition Status
Upon examination of the visual details, screen quality, and technical labels, it is understood that the product is original. The general condition of the device is good, showing signs of previous use.
Physical Deformation and Mechanical Components
There are slight signs of use on the device casing and the keypad on the front, along with localized discoloration and dirt accumulation on the key surfaces. No fractures or cracks are visible on the mechanical components or the keypad. The keys are physically intact.
Electronic Components and Screen Analysis
The electronic parts of the device are functional, and there is a backlit LCD screen on the front. The screen is active and displays a battery icon in the top left corner, program code P001, F values, duration 020, a pause indicator, and graphical bars showing channel levels. The battery icon indicates that the device is powered or shows the battery status.
Accessory Inventory and Quantity Information
The total number of products and accessories in the images has been carefully counted. The package contains 1 main device, 2 black connection cables (with red and black pins at the ends), and 1 black charging adapter/power supply. The connection cables and the adapter are bundled.
Battery Status and Power Data
The rear label of the device contains the marking: Battery Pack: 800mA 4.8Vdc. The internal battery compartment is located at the back of the device with a cover; no physical deformation such as swelling or leakage is clearly visible from the image.
Label and Text Inventory
All texts and technical data read from the images are as follows: On the front, GLOBUS, DUO TENS, P001, F, PAUSE. On the rear label, Model: DUO TENS, Electrostimulator Type: A3R, Max Power: 4.8Vdc 150mA, Output: 100mA (1000ohm), Battery Pack: 800mA 4.8Vdc, Power Input, Model: DK7-065-0200-EU, Input: 100-240Vac 50-60Hz 0.06A, Output: 5.8Vdc 200mA, double square insulation symbol, human figure symbol, IP22, CE 0478 mark, trash bin icon, DOMINO s.r.l. – Via Vittorio Veneto, 32 31013 Codognè (TV) – IT, and Elettrostimolatore expressions are present. The CE mark indicates the product’s compliance with European standards, and IP22 indicates the protection class against liquids and solid objects.
Usage Areas and Compatibility
The product is used for muscle stimulation, pain management (TENS), and muscle activation in physical therapy applications. It is suitable for use in medical and rehabilitation branches, as well as for physical therapy processes at home or in clinical settings. It should only be operated with the specified compatible original cables and accessories.
Dimensions, Compatibility, and Year of Manufacture
There is no numerical information in millimeters regarding the physical measurements or dimensions of the device in the images; however, it is the size of a handheld portable medical device. There is no direct year of manufacture written on the labels; when the design and label format of the device are evaluated concretely, it is understood to be a recent production.
Documents and Usage Duration
There are no printed documents such as invoices, warranty certificates, or user manuals in the images. There is no counter data on the device screen or labels indicating the total operating hours.
Existing Faults and Potential Risk Status
There is no clear evidence of a fault such as a broken part on the device body, an error message on the screen, or a severed cable in the images. No concrete risks such as crushed cables or deep rust on the casing have been observed; the general condition of the device is clean and usable.
