Secondhand Ondamed Bioresonance Device

Objective AI Report

Disclaimer: I am Medbidding AI. I am an unbiased AI robot. I have generated the following report automatically (without human intervention). The report was prepared by examining only the product images in the ad in detail. The report may contain errors. Medbidding and other parties disclaim any liability that may arise from this report or reliance on its contents. If you have any questions or notice an error in the report, please contact Medbidding engineers.

Report date: 25.12.2025

Ondamed Biofeedback and Frequency Therapy Device Analysis Report

Device Identification and Brand/Model Information

The product in the image is a health and therapy system console. During a detailed examination, the ONDAMED brand is prominently located on the lower right corner of the device’s front panel. The product is a specific pulsed electromagnetic field (PEMF) and biofeedback-based therapy device, known as the “Ondamed System”. The front panel design and the arrangement of control buttons indicate that the device is one of the brand’s classic models.

The presence of a document titled “ONDAMED HANDBOOK” in the box contents and among the accompanying materials confirms the brand identification.

Originality and General Appearance

The print quality on the product’s front face, logo placement, keypad design, and custom-designed LED screens indicate that the device is an original ONDAMED production. Furthermore, the forms of the brand-specific applicators (application apparatus) and their compatibility with the device confirm that the set consists of original parts.

Areas of Use

This device is designed for use in complementary medicine, pain management, and wellness fields. It is generally found in clinics or with private therapists. Its main function is to provide diagnosis and therapy support via biofeedback by sending low-frequency electromagnetic waves to the body. The different forms of applicators within the set are used to intervene in various areas of the body (neck, local areas, general body scan, etc.).

Quantity Information and Set Contents

The set shown in the image consists of the following parts in total:

• 1 Unit: Ondamed main control unit.
• 1 Unit: Original black, hard plastic carrying case.
• 2 Units: Grey hand applicators (probes) marked “Left” and “Right”.
• 1 Unit: Flexible, padded neck/nape applicator.
• 1 Unit: Large-surface, segmented/bellows-type matrix therapy pillow (with control knob connected to the device).
• 1 Unit: Device-connected control module (the part at the end of the matrix pillow with a rotary knob).
• 1 Unit: Spiral-bound user manual/book titled “ONDAMED HANDBOOK”.

Overall Condition and Cosmetic Condition

The device is generally in “Used” condition. The main unit’s front panel appears clean and well-preserved; the lettering is clearly legible. However, signs of use are more pronounced on the accessory parts. Superficial wear due to carrying is visible on the lock parts and surface of the black carrying case.

Physical Deformation and Cleanliness

Main Unit: No significant cracks, dents, or deep scratches have been observed on its metal casing or front panel. The lettering on the buttons has not faded.

Accessories: Particularly, noticeable dirt, dust accumulation, and discoloration are present in the crevices and on the surface of the beige/cream-colored segmented matrix pillow located at the bottom. Similarly, use-related dirt is visible on the gripping areas of the hand applicators. Although the neck applicator’s cover appears cleaner, it might require cleaning.

Electronic and Screen Analysis

It has been determined from the image that the device is in working condition (on). The following details regarding its electronic status have been observed:

• Upper Display: The numbers “11.64” are displayed brightly and completely on the green LED screen. No pixel loss is observed.
• Lower Display: The number “0” is clearly visible on the green LED screen.
• Indicator Lights (LEDs): The A1, A2, A3 application lights on the left side of the device and the “POWER” light in the lower right corner are illuminated in green. Additionally, the “Right” and “Left” lights in the Frequency section and the indicators in the Timing section appear active.

Mechanical Components

The push buttons on the main unit and the grey rotary knob (potentiometer/dial) on the module connected to the matrix applicator appear physically sound. The carrying case’s hinge and lock mechanisms are in place, but there might be slight paint chipping on the metal parts.

Accessories and Connections

The system possesses the basic applicator accessories required for therapy. No sheath stripping or breaks have been detected on the visible parts of the cables, but their full lengths cannot be seen in the image. The connection points of the hand probes appear robust.

A “CHIP CARD” slot is present on the main unit; however, no card is visible inserted in the image. Whether the card is included in the set cannot be confirmed from the image.

Label and Technical Information

The English technical terms and function groups located on the front panel are as follows:

• APPLICATION: Application selection (A1, A2, A3, A4 buttons).
• FREQUENCY: Frequency settings (Hz-LEFT, Hz-RIGHT buttons).
• TIMING: Timing settings (DELAY, m/s, INT buttons).
• PROGRAM: Program selection and chip card slot.

Documents

Included with the product is a “HANDBOOK” (User Manual) that appears to be original, is spiral-bound, has a blue cover, and features a large Ondamed logo. This document is an important element that adds to the product’s value, as it provides information about the device’s usage and protocols.

Potential Malfunction Risk

Although the device responds electrically and powers on, the contamination in the accessories (especially the matrix pillow) suggests the product has been used intensively. The possibility of unseen internal breaks or loose connections at cable connection points (bent areas) should always be taken into consideration. Apart from this, in terms of external appearance, there is no hazardous condition (rust, heavy impact, etc.) on the device’s body. Its condition is in line with second-hand medical device standards.