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: 10.06.2026
Report code: 1781106395
RESPIROX SZ-5AW Oxygen Concentrator Analysis Report
Device and Accessory Identification
The images show a white, vertical-design oxygen concentrator device. On the front of the device, there is a humidifier bottle, a flowmeter, an oxygen outlet, and a nebulizer interface. On the top, there is a screen and control buttons. A power cord outlet is visible at the back of the device.
Brand and Model Information
The RESPIROX brand and SZ-5AW model information are clearly stated on the label on the front of the device and on the technical information label on the side.
Authenticity Assessment
When examining the logos on the device, the print quality of the labels, and the general workmanship details, the impression is that the product is original. The detailed technical information on the labels and the CE mark support this.
Usage Areas
As understood from the “OXYGEN CONCENTRATOR” inscription, this device is a medical device that provides high-purity oxygen to users by separating oxygen from ambient air. It is suitable for use at home or in a clinical setting for chronic lung diseases such as respiratory failure, COPD, or other conditions requiring oxygen support. Thanks to the nebulizer interface, it can also be used for the administration of medication via inhalation.
Quantity Information
- Oxygen Concentrator: 1 unit
- Humidifier Bottle: 1 unit (attached to the device)
- Power Cord: 1 unit (connected to the device, the plug is not visible)
General Status and Condition
The general condition of the device is considered used. There is slight dust on the top surface and the general casing. However, no significant wear or severe damage has been observed. The screen is seen to be in working order and displaying information.
Physical Deformation
No significant scratches, dents, cracks, or color fading have been detected on the device’s casing, screen, or other visible surfaces. There are slight dust deposits on the surfaces.
Mechanical Components
The flowmeter appears to be intact and shows a value in the 0-5 L/min range. The humidifier bottle is attached to the device and contains some liquid. The control buttons and the power switch appear to be physically intact.
Electronic Components
The device’s screen is operational and displays “Cumulative time”, “Single run time”, and “Timer set” information. A green light is illuminated in the top right corner of the screen. Additionally, a yellow triangle and a red bell icon are visible, which may be warning or alarm indicators.
Accessories
A humidifier bottle is attached to the device. A power cord is seen connected to the device at the rear. No other accessories or cables are present in the image. There are “Oxygen outlet” and “Nebulizing Interface” socket inputs on the front of the device.
Battery Status
No internal or external battery is visible in the images. It is understood that the device operates while connected to the electrical grid.
Label Information
- Type: OXYGEN CONCENTRATOR: Indicates the type of device. It shows that it is a device that produces oxygen from ambient air.
- Model: SZ-5AW: The specific model code of the device.
- Power Supply: 220V +22V, 50Hz ± 1Hz input power: 500VA: Specifies the electrical supply requirements for the device to operate. It indicates 220 Volts alternating current, 50 Hertz frequency, and 500 Volt-Ampere power consumption.
- Oxygen Purity: The purity of the oxygen concentrator is 93% ± 3% when the flowrates is at between 0-5L/min: States that the device provides 93% ± 3% oxygen purity at a flow rate of 0-5 liters/minute.
- Weight: 24 Kgs: Indicates that the weight of the device is 24 kilograms.
- Output pressure: 40kPa – 70kPa: States that the output oxygen pressure of the device is between 40 and 70 kilopascals.
- Size: H55.6xW28.5xD47cm: Specifies the dimensions of the device as height (55.6 cm), width (28.5 cm), and depth (47 cm).
- SN: KA210009213: The unique serial number of the device. Used for tracking and identification of the product.
- EC REP: Prolinx GmbH: Indicates the authorized representative firm in the European Union.
- Importer: ECZACIBAŞI PAZARLAMA VE MEDİKAL SAN. TİC. A.Ş.: Indicates the importer firm of the device in Turkey.
- Made in P.R.C.: Indicates that the device was manufactured in the People’s Republic of China.
- CE 0123: The mark indicating that the device complies with European Union health, safety, and environmental protection standards. 0123 is the identification number of the notified body.
- Manufacturing Date: 11/2021: Indicates that the device was manufactured in November 2021.
- Temperature Range (-20°C to 60°C), Humidity Range (10% to 93%), Atmospheric Pressure (700hPa to 1060hPa): Environmental limits indicating safe operating and storage conditions for the device.
Screen Analysis
The device’s LCD screen is active and displays three different lines of information:
- Cumulative time: 07293 hrs: Indicates the total operating time of the device in hours. This shows that the device has been used for 7293 hours.
- Single run time: 000 min: Indicates the duration of the current single operating cycle in minutes. It currently shows zero minutes.
- Timer set: — min: Indicates the timer duration set for the device in minutes. It currently shows that no timer is set.
A green indicator light is illuminated on the right side of the screen. Additionally, a yellow warning triangle and a red bell icon are visible, providing visual feedback about the device’s status.
Dimensions and Compatibility
The dimensions are stated as H55.6xW28.5xD47cm on the side label of the device. These measurements provide an important reference for positioning the device in a home or clinical setting. Although it is not a portable device, it is easy to move thanks to its wheels.
Year of Manufacture
The manufacturing date is clearly stated as 11/2021 on the technical information label on the side of the device. This indicates that the device was manufactured in November 2021.
Documents
No documents such as invoices, warranty certificates, or user manuals belonging to the device are visible in the images.
Usage Duration
The “Cumulative time: 07293 hrs” information is clearly visible on the device’s screen. This indicates that the device has operated for a total of 7293 hours. This information is an important indicator of the device’s usage intensity.
Current Fault
No clear evidence of a fault, such as a broken part, error message, or severed cable that would prevent the device from operating, has been detected in the images. The fact that the screen is active and displaying information suggests that the device is functional.
Potential Fault Risk
The general condition of the device is good. No concrete situation that could pose a potential fault risk, such as serious wear, rust, or cable crushing, has been observed in the images. There are no significant defects on the outer surface of the device other than slight dust.
