Secondhand Respirox KSW-5 5L/min Oxygen Concentrator

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: 01.02.2026

RespiroX KSW-5 Oxygen Concentrator Analysis Report

Device Identification and Product Description

The examined visuals show a medical device stored within its box. Considering the structural form of the device, its components, and accompanying documents, the product has been identified as an oxygen concentrator that filters ambient air to produce pure oxygen. The product consists of components such as the main unit, power cable, nasal cannula, humidifier water bottle, and connection hose.

Brand and Model Information

The user manual shown in the visuals and the text on the device image were examined in detail, and the product’s brand and model information was determined with 100% certainty.

• Brand: RespiroX
• Model: KSW-5
• Product Type: Oxygen Concentrator

This information is confirmed by the “RespiroX” logo, the “Model: KSW-5” inscription, and the “Oxygen Concentrator” heading clearly readable on the cover of the user manual in the second visual.

Originality Assessment

Upon examining the print quality on the product’s user manual, the logo design, the internationally valid CE certification mark (CE 1639), and QR code integration, the product is assessed as original. Furthermore, the device’s design and material structure align with the brand’s standards.

Areas of Use

RespiroX KSW-5 is a medical device used in the treatment of patients suffering from respiratory failure, lung diseases such as COPD, or those who require an increase in blood oxygen saturation (SpO2). The device takes ambient air, removes nitrogen, and delivers high-purity oxygen to the patient. It is suitable for home use and clinical environments.

Quantity and Accessory Information

The visuals show a total of 1 main device and 4 pieces of accessories/equipment accompanying the device inside the box:

• 1 Oxygen Concentrator Main Unit
• 1 Power Cable (Black, EU type plug)
• 1 Humidifier Water Bottle – Connected to the device with a hose.
• 1 Oxygen Cannula (Inside the package, transparent green color)
• 1 User Manual Booklet

General Condition and State

The device is shown within its own box and with its accessories. The device’s casing is spotless, with no dust, yellowing, or signs of use visible. The transparency of the humidifier bottle and the unopened appearance of the cannula’s packaging indicate that the product is either new (unused) or open box (unopened but unused).

Physical Deformations and Cosmetic Examination

No cracks, breaks, dents, or deep scratches have been detected on the visible top surface and side panels of the product. The color of the plastic components is white, and no discoloration (yellowing) has been observed. The carrying handle appears sturdy.

Mechanical and External Component Analysis

• Carrying Handle: An integrated carrying handle is located on the top part of the device, which is sturdy and intact.
• Control Panel: A mechanical rotary knob with ‘+’ and ‘-‘ signs, used for flow adjustment, is present on the upper right corner of the device.
• Connection Ports: A metal or hard plastic outlet port labeled “Oxygen” is located at the bottom of the device. A white hose leading to the humidifier bottle is currently connected to this port.

Electronic Components and Display

The device’s control panel features a dark-colored display area. Since the device is not operational (it is off), digital data, operating hours, or warning lights cannot be displayed on the screen. However, the physical integrity of the display panel is complete, with no cracks or stains on it.

Battery Status

This type of oxygen concentrator (5 Liters/min capacity for home use) typically operates directly from mains electricity. No internal battery compartment or portable battery kit is visible in the visual. It draws power through the black power cable located next to it.

Detailed Analysis of Accessories

The accessories included in the box appear to be fully compatible with the device:

• Power Cable: Black in color, coiled, with a 2-pin plug suitable for Turkish standards (Type C/F compatible). No crushing or breakage is visible.
• Oxygen Cannula: Appears to be a “Nasal Oxygen Cannula” with a greenish hose, inside a transparent bag. The inscription “SIZE: Adult” on the package indicates that the product is suitable for adult use.
• Humidifier Bottle: A transparent reservoir water bottle with a brown lid. It ensures the oxygen is humidified before being delivered to the patient. The connection hose is attached to the “Oxygen” outlet.

Label and Document Information

The user manual and packaging contain the following critical information:

• Document Title: RespiroX – Oxygen Concentrator – Model: KSW-5 – User Manual.
• Certification: “CE 1639” approval is visible in the lower left corner of the manual in the second visual.
• Language Option: The manual cover features both English (“User Manual”) and Turkish (“Oksijen Yoğunlaştırıcı – Kullanım Kılavuzu”) inscriptions.
• QR Code: A QR code is present in the lower right corner of the manual, along with the inscription “For Installation and Usage Video.”
• Device Information on Manual: The image on the manual cover shows the inscription “5 LITERS,” which confirms the device’s capacity.

Size and Compatibility

The inscription “SIZE: Adult” read on the cannula packaging proves that the current cannula set is for adults. However, the device may also be suitable for use by children if appropriate pediatric accessories are acquired.

Current Malfunction and Risk Analysis

As a result of the visual analysis, no signs of malfunction such as broken parts, detached cables, oxidation, or liquid contact traces were found on the device. The general condition of the device is excellent. No potential malfunction risks (e.g., cable fraying) have been observed. The device has been physically assessed as being in “Ready for Use” condition.