Secondhand Canon CF-1 Digital Retinal Camera

Objective AI Report

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Report date: 03.01.2026

Canon CF-1 Digital Retinal Camera Analysis Report

Device Description and Brand/Model Information

The device shown in the visuals is a medical imaging system used in the field of ophthalmology (eye health). The identification information obtained from detailed inspections of the device is as follows:

• Device Type: Digital Retinal Camera
• Brand: Canon
• Model: CF-1
• Full Model Name: Canon CF-1 Digital Retinal Camera

The “Canon” logo and “CF-1 Digital Retinal Camera” inscription are clearly visible on the device’s side body and control panel. The product’s design language, optical head structure, and control panel layout indicate that this model is an original Canon product.

General Condition and Physical Condition

The device is in a used condition and shows signs of wear. The physical condition analysis is as follows:

• Body: The device’s plastic casing shows yellowing and discoloration over time. In the area of the ventilation grilles on the upper part, adhesive residue and a paper remnant, appearing to be from an old sticker or tape, are visible. No major cracks or breaks have been detected on the casing, but there is cosmetic wear due to use.
• Control Panel: The keypad and joystick area appear robust. The inscriptions on the buttons (COLOR, RED FREE, FLUO, CHIN REST, etc.) are legible; there is no fading.
• Chin Rest Unit: Superficial abrasions caused by use are noticeable on the part where the patient places their chin and on the forehead rest band.

Electronic Components and Operational Status

Visual data regarding the device’s electronic status is as follows:

• Power Indicator: In one of the visuals, the green “POWER” LED indicator, located on the bottom right of the device’s control panel, is observed to be lit. This indicates that the device is receiving power and that the power circuit is active at least at the input level.
• Controls: There is no visible missing part or physical damage on the joystick unit, trigger button, or potentiometer knobs (e.g., illumination intensity adjustment).

Mechanical Components and Optical Structure

Upon examining the device’s moving parts and optical components:

• Joystick Control: The joystick unit, which enables the device’s positioning, is in place.
• Focusing Wheels: The focusing knob and diopter adjustment mechanisms located on the side of the device are present. The + (plus), 0, and – (minus) signs for diopter adjustment are clearly visible on the side panel.
• External Fixation Lamp: An external fixation lamp, mounted on the top part of the device at the end of an articulated arm, is present.
• Cabling: A tangled appearance dominates the cables emerging from the rear and sides of the device. No visible breaks or crushes have been detected in the outer insulation of the cables, but their disarray may require detailed organization.

Accessories and Connection Units

The parts identified in the visuals, in addition to the main unit, are as follows:

• Quantity Information: 1 main device (body, optical head, and base unit), 2 external power adapters (black boxes), and their associated cable sets.
• Power Adapters: Two black power adapters/transformers are located on the ground next to the device. The cables emerging from these adapters are connected to the device. The labels on the adapters are legible, but voltage values cannot be clearly distinguished from this distance.
• Connection Sockets: Exposed connector ends are visible around the control panel (likely for camera data transfer or PC connection).

Labels and Other Information

The informational labels found on the device are as follows:

• Service/Dealer Label: A green-white label with the inscription “LASER VISION” is located on the front surface of the device’s base. This suggests that the device may have previously undergone inspection by a technical service or distributor.
• Auction/Stock Label: Temporary stock labels, secured with paper tape, featuring handwriting and a barcode (e.g., “Troostwijk”), are present on the optical head of the device.

Areas of Use

This device is a professional medical equipment. Its primary purpose is to capture photographs of patients’ retina (fundus). It is used by eye specialists (ophthalmologists) in hospital eye clinics or private clinics for the diagnosis and monitoring of diseases such as diabetic retinopathy, glaucoma, and macular degeneration.

Potential Risk and Malfunction Assessment

Based on visual inspection:

• No protective cover is visible on the optical lens portion (front lens) of the device. There is a risk of dust accumulation on the optical surfaces.
• The cable clutter and exposed connector ends indicate that caution should be exercised during installation.
• Although the device’s “POWER” light is on, optical image quality or sensor status are functional characteristics that cannot be determined by visual analysis. There is no physical heavy damage or signs of rust, suggesting that the overall condition is “medium-good”.