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Secondhand Aerti Soulfix AE-5-W 5L/min Oxygen Concentrator
Price: USD$ 270,00 Approx: 11.610,00 TL
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Shipping
Standard Shipping Conditions
In order to ensure secure transactions on Medbidding, the shipping process is managed through four different scenarios depending on the location of the buyer and seller. Free shipping is available for some categories. The terms below apply to all categories unless otherwise stated.
Buyer and Seller in Turkiye
- Seller → Medbidding: The seller packages the product and sends it to the Medbidding operations center. The seller is responsible for this shipping cost.
- Medbidding → Buyer: The product, inspected by Medbidding engineers, is sent to the buyer's address. The buyer is responsible for this shipping cost.
Buyer Outside of Turkiye, Seller in Turkiye
- Seller → Medbidding: The seller packages the product and sends it to the Medbidding operations center. The seller is responsible for this shipping cost.
- Medbidding → Buyer: The product, inspected by Medbidding engineers, is sent to the buyer's address. The buyer is responsible for this shipping cost.
Buyer in Turkiye, Seller Outside Turkiye
- Seller → Medbidding: The seller packages the product and sends it to the Medbidding operations center. The seller is responsible for this shipping cost.
- Medbidding → Buyer: The product, inspected by Medbidding engineers, is sent to the buyer's address. The buyer is responsible for this shipping cost.
Buyer and Seller Outside Turkiye
- Technical Inspection: Technical inspections are performed by our business partner in the seller's country (where available) or by our engineers via remote video call.
- Seller → Buyer: The seller packages the product and sends it to the buyer's address. The seller is responsible for this shipping cost.
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: 29.10.2025
Soul Fix AE-5-W Oxygen Concentrator Analysis Report
Overview and Device Identification
The product shown in the images is a Soul Fix AE-5-W model oxygen concentrator. The device is designed to separate oxygen from ambient air to produce medical oxygen for users who require respiratory support. This report is based on one oxygen concentrator and an attached humidifier bottle, as seen in the images.
Brand and Model Information
On the front surface of the device, the Soul Fix brand name and immediately below it, the AE-5-W model code are clearly visible. This information unequivocally identifies the product.
Usage Status and Duration
It is clearly understood from the active digital display on the front panel that the device has been used. According to the information on the screen:
- Total Operating Hours: The phrase “Total 00346 h” indicates that the device has been used for a total of 346 hours to date.
- Current Session Duration: The phrase “Run 00h:00min” indicates that the device was not operating at the time of inspection or that the session had been reset.
Physical Condition and Deformity
The overall physical condition of the product is good, despite being used. There are no visible cracks, breaks, or serious scratches on its dark gray plastic casing. However, transparent packing tape has been wrapped around the device’s body. The reason for this tape’s application cannot be determined from the images. On the control panel, the protective gelatin, believed to be factory-applied, is still present and shows some air bubbles. It is understood that the device’s wheeled structure allows for easy transport.
Electronic and Mechanical Component Analysis
The electronic components of the device are in working condition. It was observed that the blue-backlit LCD screen on the front panel clearly displays data, and the “I/O” (Power) and “O₂” (Oxygen) indicator lights on the panel are illuminated in green. The “+”, “-“, “M”, and power buttons located on both sides of the panel are physically in place. The flowmeter, a mechanical part of the device used to adjust the oxygen flow per minute, also appears to be intact.
Accessories and Connection Points
The primary accessories accompanying the device in the images are as follows:
- Humidifier Bottle: The transparent water container, which humidifies oxygen for delivery to the user, is attached to its place on the side of the device.
- Connection Tubing: A short, white connection tube is present between the device’s oxygen outlet port and the humidifier bottle.
A transparent bag is taped to the carrying handle on top of the device, but its contents are not visible. Other accessories necessary for the device’s operation, such as the electric power cord or the nasal cannula that delivers oxygen to the user, are not seen in the images.
Label and Warning Information
On the lower section of the control panel, there is an English “WARNING” label supported by various pictograms. This label contains important instructions for the safe use of the device:
- Should not be used with open flames or cigarettes.
- Oil or grease should not be used.
- Must be operated in a clean environment free from corrosion and toxic gases.
- The device’s covers should not be opened by unauthorized personnel.
- In case of an alarm, authorized service or the manufacturer should be contacted.
Other technical labels indicating the device’s serial number, REF code, or lot number cannot be discerned in the images.
Potential Malfunction Risk and Conclusion
The device’s total usage time of 346 hours indicates it has been used sparingly. The smooth operation of its electronic screen and the absence of significant physical damage suggest that the product’s overall condition is good. The presence of packing tape wrapped around the body is a notable detail, but based on the images, there is no evidence to suggest this condition results from a malfunction preventing the device’s operation. Currently, no indication of a functional issue with the device has been observed.








