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Secondhand Medelsan Galvani Faradi Device
Price: USD$ 945,00Yaklaşık: 40.635,00 TL
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Shipping
Standard Shipping Conditions
In order to ensure secure transactions on Medbidding, the shipping process is managed through four different scenarios depending on the location of the buyer and seller. Free shipping is available for some categories. The terms below apply to all categories unless otherwise stated.
Buyer and Seller in Turkiye
- Seller → Medbidding: The seller packages the product and sends it to the Medbidding operations center. The seller is responsible for this shipping cost.
- Medbidding → Buyer: The product, inspected by Medbidding engineers, is sent to the buyer's address. The buyer is responsible for this shipping cost.
Buyer Outside of Turkiye, Seller in Turkiye
- Seller → Medbidding: The seller packages the product and sends it to the Medbidding operations center. The seller is responsible for this shipping cost.
- Medbidding → Buyer: The product, inspected by Medbidding engineers, is sent to the buyer's address. The buyer is responsible for this shipping cost.
Buyer in Turkiye, Seller Outside Turkiye
- Seller → Medbidding: The seller packages the product and sends it to the Medbidding operations center. The seller is responsible for this shipping cost.
- Medbidding → Buyer: The product, inspected by Medbidding engineers, is sent to the buyer's address. The buyer is responsible for this shipping cost.
Buyer and Seller Outside Turkiye
- Technical Inspection: Technical inspections are performed by our business partner in the seller's country (where available) or by our engineers via remote video call.
- Seller → Buyer: The seller packages the product and sends it to the buyer's address. The seller is responsible for this shipping cost.
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: 05.09.2025
Medelsan Reo-Cro Galvanifaradic Sinusoidal Device Analysis Report
Overview and Device Identification
The device shown in the visuals is an electrotherapy instrument. From the inscription “GALVANİFARADİ SİNÜZOİDAL” on it, it is understood that it is a device used in the field of physical therapy and rehabilitation. The analysis covers a total of 1 main unit, 1 power cable connected to the device, and 1 patient output cable found in the visuals. Considering the logo print on the product, the clarity of the texts, and the overall craftsmanship quality, it is evaluated as original.
Brand and Model Information
During the detailed examination, brand and model information clearly readable on the device’s front panel was identified. According to this information, the device’s brand has been confirmed as Medelsan and its model as Reo-Cro.
Physical Condition and Deformation Analysis
The device is generally in a used but well-preserved condition. No noticeable scratches, cracks, dents, or discoloration have been observed on its light-colored casing. Only minimal, insignificant marks due to use are present on its surface. The overall cleanliness of the device is good, and there is no significant dirt or dust accumulation. There is slight wear on the front control panel; particularly, a slight fading and abrasion are observed on the red painted parts of the “Tp” and “Ti” adjustment knobs. However, this condition is not a deformation that would affect the device’s functionality.
Mechanical and Electronic Component Examination
The mechanical components of the device are visually in good condition.
- Buttons and Switches: All adjustment knobs (potentiometers), up-down directional buttons, and the polarity change switch (toggle switch) located on the device’s front panel are physically complete and sound.
- Casing and Ventilation: The integrity of the device casing is complete. There are no broken or cracked parts.
- Electronic Components: Although the internal electronic components of the device are not visible in the visuals, no damage or burn marks have been detected on electronic components such as the screen and connection points when viewed from the outside.
Accessories and Connection Points
The following accessories have been identified with the device in the visuals:
- Power Cable: There is one power cable exiting from the back of the device, equipped with a grounded plug. No crushing or tearing is observed in the cable’s insulation.
- Patient Output Cable: There is one patient electrode cable, plugged into the socket at the front bottom of the device, with red and black banana-type connectors at its ends. The cable is visually in good condition.
The device has one multi-pin female socket input for the patient cable. No electrode pads or other accessories are present in the visuals.
Control Panel and Screen Analysis
The device’s front control panel features one digital screen and various adjustment knobs.
- Screen: The digital timer screen displays the numbers “88”. This is typically a state used by 7-segment displays to show that all segments are functioning during power-on or in test mode. Below the screen, the inscription “min.” is located, indicating that this screen shows the therapy duration in minutes.
- Controls: The panel features rotary knobs for adjusting the current type (F1, F2, FMOD, S, E1, G, KG), current intensity (0-100 mA), pulse and pause durations (“Tp” and “Ti”), and a polarity selection switch (+ = +, + = -).
Potential Risk Assessment
Based on the examination of the visuals, the overall condition of the device appears to be quite good. No crushing, peeling, or exposed wires are found in its cables. The absence of any serious impact or breakage on its casing suggests that the internal components are protected. Other than the slight cosmetic wear on the adjustment knobs, no clear visual evidence indicating a risk of device malfunction has been detected. The current physical state of the product indicates regular use.