Secondhand Erbe ICC 50 Electrocautery Machine

Objective AI Report

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Report date: 11.12.2025

ERBE ICC 50 Electrosurgery Unit Analysis Report

Brand and Model Information

A detailed examination of the product in the visual has revealed that the device’s brand is ERBE, clearly written in blue font in the upper left corner. Immediately below the brand name, the inscription ICC 50, written in grey font, precisely indicates the device’s model. Warning texts such as “Fehldosierung / Output Error” on the panel, in both German and English, reflect ERBE’s German-originated engineering design language.

Originality Status

The front panel design, button placements, color codes (yellow for cut, blue for coagulation), logo print quality, and typography of the device completely match an original ERBE medical device. No signs of imitation or aftermarket parts have been found. The device has an original casing compliant with industrial and medical standards.

Product Type and Areas of Use

This device is an electrosurgery unit (cautery device) used in medical procedures. The ports and control panel on the device indicate that it is designed for the following operations:

• Cut: Tissue cutting procedures (options “Effect 1” and “Effect 2” are available on the yellow panel).
• Coag (Coagulation): Bleeding control procedures (options “Forced”, “Soft”, and “Bipolar” are available on the blue panel).
• Bipolar Mode: Precise surgical procedures using bipolar forceps.

Its compact structure (ICC 50 model) is generally suitable for use in dermatology, polyclinic surgery, minor surgical interventions, and outpatient treatment units.

General Condition and Physical Deformations

The device is in second-hand (used) condition. Notable details from the physical inspection are as follows:

• Front Panel Surface: On the label of the yellow “CUT” section, noticeable surface scratches and friction-related wear are observed, especially around the screen and buttons. However, these abrasions have not rendered the text unreadable.
• Casing Integrity: No visible cracks, fractures, or major dents have been detected on the device’s grey outer casing.
• Socket Inputs: In the cable input ports at the bottom (Neutral, Cut/Coag, Bipolar), slight discoloration and dust accumulation due to use are present.

Control Panel and Screen Analysis

The device’s control interface has been thoroughly examined in the visual:

• Left Warning Area: A red LED warning labeled “Fehldosierung / Output Error” and an “NE” light indicating neutral electrode connection are present.
• Middle Panel (Yellow – CUT): Dedicated to cutting procedures. It features two 7-segment digital display digits (currently dim), up-down arrow keys for effect selection and power adjustment, and a mode selection button.
• Right Panel (Blue – COAG): Dedicated to coagulation procedures. It includes LED indicators for “Forced”, “Soft”, and “Bipolar” modes, and a digital power display screen.
• Power On/Off Button: In the bottom left corner, there is a rocker-type power switch, presumed to be green-lit, marked with “I/O” symbols.

Connection Ports and Compatibility

The front bottom section of the device features three main connection points:

• Neutrale: Patient plate (neutral electrode) connection input. A heart symbol (possibly a “BF” type isolation symbol) is visible next to it.
• Cut / Coag: Socket used for monopolar handpiece or footswitch connection.
• Bipolar: Dual-input socket used for bipolar cable/forceps connection.

Quantity and Accessory Information

The visual shows only 1 unit of the main unit (generator). Accessories necessary for the device’s operation, such as the power cable, patient plate, monopolar pencil, bipolar forceps, or footswitch, are not present in the visual.

Mechanical and Electronic Component Evaluation

The device’s membrane keypad maintains its integrity; there are no tears or detachments in the buttons. The power switch is in place and robust. Although the functionality of the electronic components (screens and circuits) cannot be verified from the visual as the device is powered off, no physical cracks are observed on the screen panels.

Potential Malfunction Risk

Although the device appears robust externally, the superficial wear on the panel indicates intensive use. In medical devices of this type, oxidation in the internal contacts of the sockets or a decrease in the sensitivity of the membrane keypad can occur over time. However, no critical damage that would directly impede the device’s operation (e.g., fractures, fragmented casing) has been detected in the visual. It is anticipated to be in “May Require Maintenance” condition.