Secondhand Erbe VIO 300D Electrocautery Machine

Objective AI Report

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Report date: 31.07.2025

Erbe VIO 300 D and APC 2 Electrosurgical System Analysis Report

Overview and Device Identification

The images show an electrosurgical system positioned on a medical trolley. The system consists of two main units and various accessories. The analysis focuses on this integrated system as seen in the images. Objects visible in the background that are unrelated to the product have not been included in the analysis.

The total number of parts subject to this report is listed below:

• 1 unit of Erbe VIO 300 D Electrosurgical Unit
• 1 unit of Erbe APC 2 Argon Plasma Coagulation Unit
• 1 unit of Erbe branded trolley
• 1 unit of double foot pedal (yellow and blue)
• 1 unit of metal accessory basket
• 1 unit of blue gas cylinder and its regulator
• Various connection cables and a single-use patient plate

Brand and Model

The logos and model names on the device units and the trolley are clearly visible. Based on this information, the brand and models of the devices are specified below.

• Electrosurgical Unit Brand-Model: Erbe VIO 300 D
• Argon Plasma Unit Brand-Model: Erbe APC 2

Area of Use and Authenticity

The Erbe VIO 300 D is an electrosurgical generator used for tissue cutting and stopping bleeding (coagulation) during surgical operations. The APC 2 unit is a module that provides non-contact coagulation using argon gas. The system as a whole is a professional medical device used particularly in endoscopic and open surgical procedures. Considering the print quality of the logo, the screen interface, the craftsmanship of the buttons, and the overall material quality, the product is assessed to be an original Erbe manufacture.

General Status and Condition

The general status of the device set is used but it appears to be in very good condition. No significant wear is observed on the casings of the units or on the trolley. The device gives the impression of being clean and well-maintained, and used in a professional environment.

Physical and Mechanical Assessment

Based on visual inspection, the condition of the physical and mechanical components of the device is summarized below.

• Casing and Body: There are no cracks, dents, or significant color fading on the casings of the VIO 300 D and APC 2 units. The surfaces are clean.
• Trolley: The trolley, made of metal and plastic parts, has a sturdy structure. Its wheels appear to be intact and mobile. The metal basket on it has no deformation.
• Foot Pedals: Although there is slight wear on the surfaces of the yellow and blue foot pedals due to use, no breaks or damage that would impede their function are visible.

Electronic Components and Screen Analysis

The electronic components of the device are in working order. The screen of the VIO 300 D unit is on and the display quality is clear. No pixel defects or abnormalities were observed on the screen. The power and status indicator (green and red) LED lights on the front panel are active. The illumination of the red light is typically a status alert indicating that the patient plate circuit is not complete, and does not signify a malfunction.

The following information is readable on the screen:

• Program Name: 1 CEKUM SAGKOLON POL
• Modes: ENDO CUT Q and FORCED COAG
• Parameters: Settings such as effect, power (max. 60 watts), and cutting duration/interval are visible.

This information indicates that the device’s menu is operational and has been set for a specific surgical procedure.

Accessories and Equipment

The accessories included with the system are as follows:

• Gas Cylinder: Behind the trolley, there is a blue argon gas cylinder used for the APC 2 unit. A pressure regulator is attached to the cylinder.
• Cables and Supplies: The metal basket contains various connection cables and a single-use patient plate (grounding pad) in its packaging. There is no visible crushing or damage to the cables.
• Connection Ports: The monopolar, bipolar, and patient plate input sockets on the front panel of the devices appear clean and undamaged.

Label and Technical Information

Labels containing specific technical information such as the serial number, REF code, lot number, or year of manufacture, which may be located on the rear or bottom of the devices, are not clearly legible in the images. Therefore, this information could not be included in the report.

Potential Malfunction Risk and Conclusion

In the inspection based on the available images, no obvious damage, wear, or potential malfunction risk (such as crushed cables, rust, cracks in critical parts, etc.) that would directly affect the device’s operation was detected. The overall condition of the device gives the impression of equipment that has been regularly used and maintained. Together with its accessories and main units, the system is assessed to be in good condition.