Defective Secondhand Rhinolight Phototherapy Device

Objective AI Report

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Report date: 17.12.2025

RHINOLIGHT Intranasal Phototherapy Device Analysis Report

Device Identification

The device examined in the visuals is a medical phototherapy unit designed for intranasal (inside the nose) light therapy applications, which can be mounted on a stand. From the visuals on the information leaflet located on the left side of the device and its general form, it has been determined that it is used to deliver light of a specific wavelength to the nasal mucosa for the treatment of allergic rhinitis.

Brand and Model

The brand is clearly and legibly displayed on the front of the device and on the upper information leaflet.
Brand: RHINOLIGHT
Manufacturer Information: Rhinolight Ltd. (located in Szeged, HUNGARY)
Model: Although a specific model number (e.g., “IV” or “Semiconductor”) is not explicitly written on the device casing, the product is characteristic clinical type phototherapy device of the brand.

Originality and Origin

The laminated leaflet titled “Medical Therapy Protocol” located next to the product contains the full address of the manufacturer (14 Jankovich str, Szeged 6726, HUNGARY) and contact information. Furthermore, the leaflet includes the CE 1011 certification mark and SGS quality control logos. The device’s mold craftsmanship, the print quality of the logos, and the warning labels indicate that the product is an original RHINOLIGHT device.

Areas of Use

This device is used to apply high-intensity light to the nasal mucosa for the relief of allergic rhinitis (hay fever) symptoms. The diagram in the information leaflet visualizes the application to the nostrils via a probe. It is suitable for professional use in Ear, Nose, and Throat (ENT) clinics and allergy treatment centers.

Quantity Information

The visuals show 1 unit of the RHINOLIGHT main control unit and 1 unit of the carrier stand body to which this unit is mounted.

General Condition and Physical Deformation

The device is in a second-hand and used condition. Detailed observations regarding its physical state are as follows:

• Color Change: There is a noticeable yellowing (discoloration due to corrosion or UV effect) on the beige/cream colored central plastic body and top cover of the device. The green plastic parts on the sides have retained their color tone better.
• Dirtiness: A layer of dust and dirt is observed accumulated in the indentations on the top surface of the device, at the edge joints, and around the buttons. It requires a detailed external cleaning.
• Structural Integrity: No significant deep cracks, breaks, or dents have been detected on the outer casing. The casing integrity is preserved.

Electronic Components and Screen Analysis

A square-shaped LCD screen is located on the front of the device. Since the device is turned off (unpowered), the screen appears black; therefore, no comments can be made about pixel errors or operational status based on the visual. However, no deep scratches or cracks are visible on the screen glass.

Mechanical Components and Keypad

The control panel consists of a total of 6 physical buttons located to the right and left of the screen.
Left Panel: Plus (+), Lamp Symbol, Minus (-)
Right Panel: Play, Power, Stop
The symbols on the buttons are legible; there is no fading. The keypad appears physically sound.

Accessories and Missing Parts

The most critical point identified during the analysis is the condition of the treatment heads (probes):

• Risk of Missing Parts: Probe slots (socket inputs/holders) are present on the right and left sides of the device. However, no light therapy cable or hand probe that should be attached to these slots or connected to the device is visible in the visuals. These parts are essential for the device to perform its main treatment function.
• Stand: The device is mounted on a gray-colored stand labeled “MDT” (presumed to be height-adjustable). Only the upper neck portion of the stand is visible.
• Information Card: The original usage protocol leaflet is present on the side table next to the device.

Label and Document Information

The texts on the information leaflet in the visual have been analyzed:

• Document Type: Medical Therapy Protocol
• Application Information: Contains instructions regarding the frequency of treatment application during the first week and session durations.
• Warnings: Medical warnings such as “Use vitamin A oil if dryness occurs in the nasal mucosa” and “Eyes must be protected” are included.
• Certificates: CE1011, SGS, ISO logos are present on the document.

Potential Malfunction Risk

The yellowing on the outer casing of the device indicates prolonged use or exposure to sunlight. However, there is no rust or damage that would cause the casing to open. The absence of the light probe (handpiece), which is necessary for the device’s operation, in the visual creates the risk that this part may be lost or stored separately. The buyer must definitely inquire about the probe’s condition.

Conclusion

The examined RHINOLIGHT brand phototherapy device is a medical product that physically maintains its integrity but cosmetically shows wear and tear due to use (yellowing and dirtiness). While the main body of the device and the stand connection are present, the wired probe unit that enables the treatment application is not visible in the visuals. The presence of the original usage instruction leaflet is an advantage.