6 Pieces Secondhand Coblator II Radiofrequency Surgical Unit

Objective AI Report

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Report date: 21.07.2025

ArthroCare Coblator SPINE and Coblator II Analysis Report

Device Identification and Quantity Information

In the images, there is a group of electrosurgical units designed for use in medical procedures, along with various accessories for these units. The products are neatly arranged on a shelving system. The total quantity information is as follows:

• 6 ArthroCare Coblator SPINE units
• 1 ArthroCare Coblator II unit
• 1 Triple (Reverse, Oscillate, Forward) foot pedal
• At least 2 single-use surgical probes/wands in sterile packaging
• Boxes of medical consumables from various brands
• 2 transparent plastic storage containers/trays

Brand and Model

The brand and model of the main devices and some accessories in the images have been clearly identified:

• Main Device Brand-Model: ArthroCare Coblator SPINE
• Secondary Device Brand-Model: ArthroCare Coblator II
• Foot Pedal Brand-Model: ArthroCare (The model is not specified on the pedal, but it appears to be compatible with the devices.)

Additionally, a product box from the brand “U&SURE” is visible, but its contents could not be fully identified.

Authenticity and Area of Use

The logo (“ArthroCare”), model names (“Coblator SPINE”), the quality of button and screen prints, craftsmanship details, and overall appearance of the devices strongly indicate that the products are original. Coblator systems are radiofrequency-based surgical devices used for the controlled ablation (dissolving/removing) and coagulation (stopping bleeding) of soft tissue. The “SPINE” designation indicates that these devices are specifically designed for use in spine surgery procedures. The foot pedal is used to control the device’s functions (e.g., forward, reverse, oscillation) during the surgical procedure. The probes in sterile packaging are single-use consumables used during these procedures.

General State and Condition Assessment

All devices and accessories in the images are assessed as lightly used and in very good condition. All products are stored in a clean, orderly, and well-maintained environment. There is no significant wear, dirt, or dust on the device casings. This indicates that the devices have been used and maintained with care.

Physical and Mechanical Condition

In the visual inspection, no significant physical deformation was detected on any of the devices. The casing, buttons, switches, ventilation grilles, and socket inputs on the front panel are all intact and clean. No cracks, breaks, dents, or discoloration were observed on them. The plastic components and pedal mechanisms of the foot pedal also appear to be in good working order. All mechanical parts have a functional and undamaged appearance.

Accessories and Complementary Products

There are various accessories included with the device set. The set includes a triple foot pedal of the ArthroCare brand, which controls the devices. Additionally, there are at least two surgical probes in their sterile packaging, which appear to be unused. In the images, there are also several cardboard boxes containing medical supplies, one of which is branded “U&SURE”. The presence of these boxes suggests that consumables for use with the devices may also be available. There is no evidence of any missing parts or accessories.

Label and Box Information

The “U&SURE” branded box shown in the images has various label information and symbols on it. Among these symbols, the CE mark and signs indicating single-use can be seen. Although there are areas on the box for information such as REF (Reference Code) and LOT (Lot Number), the image resolution does not allow for these codes to be read clearly.

Potential Malfunction Risk Assessment

Based on the visual inspection, no severe wear, corrosion, crushed cables, or critical damage that could lead to an imminent malfunction has been observed on the devices. The overall condition of the devices is very high, indicating they are ready for regular use. This stated assessment is a forecast based solely on visual evidence and does not imply that the devices have undergone a full functional test.