Secondhand Gyrus Acmi PK Superpulse Radiofrequency Surgical Unit

Objective AI Report

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Report date: 21.01.2026

Gyrus ACMI PK SuperPulse Electrosurgical Unit Analysis Report

Device Identification

The main product shown in the visuals is an energy platform used in surgical operations. This device is an electrosurgical generator used for tissue cutting (cut) and coagulation procedures in medical procedures. A footswitch unit connected to the device is also located on the unit.

Brand and Model

As a result of a detailed examination of the device’s front panel, brand and model information has been definitively identified:

• Brand: GYRUS ACMI (Clearly readable on the label on the front left panel.)
• Model Series: PK SUPERPULSE (The model name located on the front right panel along with the logo.)

The device’s brand has been verified as GYRUS ACMI and its series as PK SUPERPULSE.

Originality

Considering the “GYRUS ACMI” logo, “PK SUPERPULSE” graphics, button structures, industrial design quality, and its distinctive orange casing color on the product, the product is evaluated to be an original medical device.

Applications

This device is designed for use in professional surgical interventions. It is particularly used in urology (TUR, prostate operations) and gynecology branches to provide tissue resection and hemostasis with “Plasma Kinetic” technology. The yellow and blue pedals allow the surgeon to control cutting and coagulation procedures with their foot.

Quantity Information

A total of 2 main parts, integrated or connected by cable, are visible in the visual:

• 1 Gyrus ACMI Generator Main Unit
• 1 Dual Footswitch (Cut/Coag)

Overall Condition

The device is in used condition (second-hand). There are cosmetic marks on the product’s outer casing and screen surface due to use. However, the device maintains its integrity and does not have a heavily damaged appearance.

Physical Deformation

The physical condition of the product has been analyzed with visual data as follows:

• Upper Casing: On the orange-colored upper metal/plastic casing of the device, prominent white scuff marks and scratches are present, especially in areas near the left side.
• Screen Surface: Numerous superficial scratches due to use have been detected on the protective glass/plastic surface of the LCD screen on the front panel.
• Edges: Minor abrasions in the device’s paint have been observed in places.
• Pedals: Although the surfaces of the footswitches appear clean, it is evident that they have been used.

Mechanical Components

The membrane keypad located on the front panel (on/off button, up/down arrow keys) appears physically intact. The footswitches maintain their integrity; no breaks or cracks were detected in the pedals in the visual. The colors of the pedals (Yellow and Blue) are distinct.

Electronic Components

The device’s screen is off in the visual, therefore the operational status of the pixels or whether the device is displaying an error code could not be analyzed. A black socket input used for prop/cable connection is present at the bottom right of the front panel and appears physically intact.

Accessories

One dual footswitch is seen with the device:

• Yellow Pedal: It is labeled “CUT” (Cutting).
• Blue Pedal: It is labeled “COAG” (Coagulation).
• Cables: A black cable harness connected to the pedals is resting on top of the device. No visible breakage or peeling of cable sheaths could be discerned in the visual.

The device’s main electrical power cord could not be clearly distinguished in this visual, only the connection cable of the pedals is visible.

Battery Status

The device typically operates with mains electricity. No internal battery indicator or an indication of portability is present in the visual.

Label Information

Texts read and label details on the product:

• Left upper label: GYRUS ACMI
• Right upper text: PK SUPERPULSE
• Pedal labels: CUT, COAG
• Socket input label: PK / SP

Screen Analysis

An LCD screen, presumed to be dot-matrix in structure, is located on the front. The screen is off (black/dark blue background). Vertical and horizontal usage scratches are present on the screen surface.

Dimensions and Compatibility

Although precise millimeter measurements cannot be given from the visual, the device is a portable desktop unit, sized appropriately for standard medical rack systems or operating room desktop use. The size of the pedals is suitable for adult human foot ergonomics.

Year of Manufacture

Since the rear label (rating plate) containing the device’s manufacturing date is not visible in the visuals, the year of manufacture could not be determined.

Documents

No invoice, warranty certificate, or calibration label was found in the visual. Therefore, it is unknown whether the device’s warranty is still active.

Usage Duration

Information regarding how long the device has been used (hours/number of operations) is not visible on the screen or an analog counter.

Current Fault

During the visual inspection, no broken parts, dented casing, severed cables, or error warnings such as “Service Required” were observed. Only cosmetic wear and tear is present.

Potential Fault Risk

The scratches observed on the product’s upper casing and screen indicate that the device has been actively used and transported. In such intensive use, the sensitivity of the front panel buttons and the contact points of the socket inputs (especially the PK/SP port) may wear out over time. Before purchase, it would be beneficial to test the device to ensure that its screen is functional and that the footswitch functions are triggering correctly. Its current physical condition indicates that the device is a second-hand product with a “high probability of being in working condition”.