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: 02.06.2026
Report code: 1780403500
RESPIRONICS EverFlo OPI Oxygen Concentrator Analysis Report
Device Identification and Brand Model Information
In the images, an oxygen concentrator used for providing respiratory support has been identified. The text “EverFlo | OPI” is clearly legible on the front and side label of the device. The “RESPIRONICS” logo is also present on the side label. In light of this information, the brand of the device has been identified as RESPIRONICS, and the model as EverFlo OPI.
The REF code of the device is stated as 1020006 on the label.
Authenticity Assessment
Upon examining the general build quality of the product, the clarity of the labels, and the precision of the logo printing, it is observed to be an original product. There are no signs of counterfeiting.
Usage Areas
This device is an oxygen concentrator designed for patients requiring oxygen therapy at home or in a clinical setting. It is used to meet the respiratory support needs of patients with conditions such as lung diseases, COPD, and heart failure. The device filters nitrogen from the ambient air to produce high-concentration oxygen and delivers it to the patient via a nasal cannula or mask.
Quantity Information
A total of two items have been identified in the images: one main device (oxygen concentrator) and one power cable.
General Condition and Physical Deformation
The general condition of the device is considered used. There are no significant scratches, dents, or cracks on the casing. However, there is slight dust and dirt accumulation around the power switch and on the general surface of the device. The “PROPERTY OF PATIENT” label on the front panel is slightly peeling at the corners.
Mechanical and Electronic Components
Regarding the mechanical components, the wheels located at the bottom of the device appear to be sturdy. The flow meter and power switch on the front panel are physically in place. LPM (Liters Per Minute) values from 1 to 5 are visible on the flow meter. The power switch and warning lights, which are visible as electronic components, are in place. There is a digital display on the upper rear part of the device.
Accessories
A black power cable is visible with the device. The cable is wrapped around the back of the device. No other accessories or spare parts are present in the images. There is an oxygen outlet socket and a slot for a humidifier bottle on the top of the device. The humidifier bottle is not present in the images.
Battery Status
No external or internal battery belonging to the device has been identified in the images. It is understood that the device operates via mains electricity using the power cable.
Label Information
- Serial Number (SN): Stated as (21) 21474707 on the label. The serial number is the unique identifier for each product and is used for production tracking, warranty processes, and service history.
- REF Code: Stated as REF 1020006 on the label. The REF code is the catalog number or reference code of the product, identifying a specific model or configuration of the product.
- Other Codes or Technical Information:
- (01)00606959032552: This code may be the GTIN (Global Trade Item Number) or a similar barcode identifier for the product.
- IP21: This code indicates the Ingress Protection classification of the device. IP21 indicates that the device is protected against solid objects larger than 12.5 mm and provides protection against vertically falling water drops.
- 220-240V~ 50Hz 1.3A: These values indicate the operating voltage, frequency, and current requirements of the device. It shows that the device operates with 220-240 Volts alternating current at a frequency of 50 Hertz and draws 1.3 Amperes of current.
- 14-15 kg: This value indicates the approximate weight of the device.
- CE Mark: Indicates that the product complies with the European Union’s health, safety, and environmental protection standards.
- cTUVus Mark: A certification mark indicating that the product complies with North American safety standards.
- Symbols: There are warning symbols on the label such as no smoking, keep away from open flames, do not use oil or grease, consult instructions, and do not dispose of with household waste.
Display Analysis
The value “24692” is read on the digital display located on the upper rear part of the device. This value indicates the total operating time of the device in hours. This information is important data for understanding how much the device has been used.
Dimensions and Compatibility
The exact dimensions of the device are not specified in the images. However, based on its general appearance and wheeled structure, it is understood to be a portable yet stationary oxygen concentrator designed for home use. The ergonomic design of the device allows it to occupy less space in a home environment and be moved easily.
Year of Manufacture
There is no direct information regarding the year of manufacture on the labels. However, considering the general design, label format, and physical condition of the device, it can be interpreted that it is a modern medical device and may have been produced in recent years. The fact that the device is used indicates that it has a certain duration of usage.
Documents
No invoices, warranty certificates, user manuals, or other documents belonging to the device are visible in the images. Therefore, no additional document information to be presented to the buyer has been identified.
Usage Duration
The value “24692” is clearly visible on the digital display on the upper rear part of the device. This indicates that the device has operated for a total of 24692 hours. This information provides concrete data regarding the intensity of the device’s usage.
Existing Faults
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 identified in the images. The general structure of the device maintains its integrity.
Potential Risk of Failure
The general condition of the device is good. No concrete situation that could pose a potential risk of failure, such as severe wear, rust, or cable crushing, has been observed in the images. Except for slight dirt and dust around the power switch, there is no condition that threatens the mechanical and electronic integrity of the device.
