Secondhand Olympus Celonlab Precision Radio Frequency Device

Objective AI Report

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Report date: 17.12.2025

OLYMPUS CelonLab PRECISION Radiofrequency Power Control Unit Analysis Report

Device Identification, Brand and Model Analysis

The main product shown in the visuals is an electronic power control unit used for medical purposes. The brand and model information on the device’s front panel is extremely clear and legible. Accordingly, the product’s brand has been identified as OLYMPUS, and its model as CelonLab PRECISION. The device is a power control unit designed for Olympus’ Celon methodology.

Product General Description and Areas of Use

OLYMPUS CelonLab PRECISION is a bipolar RF power source generally used for soft tissue coagulation and radiofrequency (RF) ablation procedures in ENT (Ear, Nose, and Throat) applications. The device is specifically designed for minimally invasive surgical procedures in snoring treatment, nasal concha reduction, and soft palate applications. Sockets on the front of the device are used for connecting appropriate bipolar electrodes and applicators.

Physical Condition and Cosmetic Examination

Visual analysis details regarding the device’s external casing and cosmetic condition are as follows:

• Case Condition: The device’s beige-colored outer casing, a mixture of metal and hard plastic, appears quite clean. There are no visible dents, cracks, rust, or deep scratches. Corners and edges are neat.
• Front Panel: The device’s characteristic blue front panel is not deformed. The texts on the panel (Power Level, Application Time, etc.) are not erased and are legible. The membrane keypad surface is intact, with no observed tears or perforations.
• Cleanliness: The product generally appears hygienic and well-maintained, giving the overall impression of having been used in a clinical environment.

Quantity and Accessory Information

The product set in the visuals consists of the following components:

• 1 unit OLYMPUS CelonLab PRECISION Main Unit
• 1 unit Black, wired Footswitch

The main power cable or patient application electrodes (probes) are not visible in the visuals. The black footswitch is positioned on the right side of the device, potentially connected to it.

Technical Interface and Control Elements Analysis

The controls and inputs on the front panel are as follows:

• Power Switch: On the left side, there is an On/Off switch, which appears to be illuminated green. The button seems mechanically sound.
• Power Level: In the center, there is a two-digit digital display (LED) area and up/down membrane buttons for power adjustment.
• Application Time: On the right side, there is a digital display area showing time in minutes and seconds (m:s). Next to it is a function button related to the timer or mode.
• Connection Ports: On the bottom left of the front panel, there is a circular (likely electrode or neutral plate input) and on the bottom right, a wider black connection port. No corrosion or broken pins are observed in the inputs.
• Symbols: Under “Power Level” and “Application Time,” there are a human figure symbol indicating “Type BF” (Body Floating) patient protection class and warning triangle icons.

Originality Assessment

Upon examining the device’s typography, color palette (Olympus’ distinctive blue tone), label placement, and material quality, the product is assessed as Original. There are no visual indications of it being a counterfeit or replica.

Mechanical and Electronic Component Status

The device is in the off position in the visuals, so it cannot be visually confirmed whether the digital screens are working (i.e., if there are any dead pixels). However:

• There is no mechanical deficiency in the buttons or switch structure.
• The footswitch appears sturdy, and its cable connection extends towards the back of the device.
• The fan grille or ventilation openings (as far as visible) are not blocked.

Potential Fault Risk and Final Comment

The product is visually in very good condition (Clean Used / Well-maintained). The absence of visible breakage, impact, or liquid contact marks indicates a low potential fault risk. However, as the device is medical electronic equipment, the calibration status of its internal electronic circuits or the lifespan of its battery/fuses can only be determined through technical service testing. In light of the visual data, it can be stated that the device’s physical integrity is preserved, and its potential for readiness for use is high.