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: 30.05.2026
Report code: 1780104432
ResMed S9 VPAP ST-A Respiratory Device Analysis Report
Device and Accessory Identification
The images show one ResMed brand respiratory device, a power adapter, a power cord, a carrying case, and a user manual/information document. The device is a medical product used to provide respiratory support.
Brand and Model Information
The “ResMed” brand is clearly visible on the front panel and the rear label of the device. The front panel features the terms “VPAP ST-A” and “iVAPS”. The rear label displays the “S9” designation and the “VPAP ST-A” model name again. Based on this information, the full model name of the device has been identified as ResMed S9 VPAP ST-A.
Authenticity Assessment
The ResMed logos on the device, the print quality of the labels, the overall workmanship, and the accompanying original carrying case and documents suggest that the product is authentic.
Usage Areas
The ResMed S9 VPAP ST-A is a respiratory support device designed for non-invasive ventilation. It is primarily used for patients with respiratory disorders such as sleep apnea or those requiring respiratory support. The device operates on a two-phase principle: IPAP (Inspiratory Positive Airway Pressure) and EPAP (Expiratory Positive Airway Pressure). With its iVAPS mode, it aims to maintain targeted ventilation by automatically adjusting alveolar ventilation. This device is typically used in pulmonology and sleep medicine departments.
Quantity Information
- Respiratory Device: 1 unit
- Power Adapter: 1 unit
- Power Cord: 1 unit
- Carrying Case: 1 unit
- User Manual/Information Documents: 1 set
General Condition
The general condition of the device appears to be good. There is no significant wear or heavy signs of use on the surfaces. The accessories are in similarly good condition.
Physical Deformations
No visible scratches, dents, cracks, or discoloration have been detected on the device’s casing, screen, or other exterior surfaces. The product has a clean and well-maintained appearance.
Mechanical Component Inspection
The power button, info button, rotary control dial, and the orange alert button on the front panel appear to be intact. The connection points and covers on the rear also show no signs of any mechanical issues.
Electronic Component Status
The device’s screen is off in the images; therefore, no electronic information or error messages on the screen could be analyzed. There are no visible abnormalities in the exterior appearance of the device’s general electronic components.
Condition of Accessories
A power adapter and power cord are included with the device. The ResMed logo is present on the power adapter, and the cables are neatly coiled. No cuts, crushing, or deformations were observed. Additionally, there is a black carrying case with the ResMed logo and a user manual/information document. The documents contain information regarding SD card usage. A SD card slot is visible on the back of the device, but no SD card is present in the images. Information regarding the expiration dates of the accessories is not provided in the images.
Battery Status
No integrated or external battery is visible in the images. Therefore, no comments can be made regarding the battery status.
Label Information
- SN (Serial Number): 22161154587. This number indicates the unique identity of the product and is used for production tracking, warranty processes, and service history.
- LOT (Lot Number): 1166625. The lot number indicates that the product belongs to a specific production batch. It allows for the identification of the relevant batch in cases of recalls or quality control.
- REF (Reference Code): 36219. The reference code indicates the catalog number or model variant of the product. It is used for order and inventory management.
- IP21: This code refers to the device’s Ingress Protection rating. The first digit (2) indicates protection against solid objects (protected against objects larger than 12.5 mm), while the second digit (1) indicates protection against water (protected against vertically dripping water).
- DC 24V, 2.5A (FG), 3.75A (Sys): These values indicate the power requirements of the device. It shows that the device operates on 24 Volts DC and draws 2.5 Amperes for the fan motor (FG) and 3.75 Amperes for the system (Sys).
- CE: This mark indicates that the product complies with the European Union’s health, safety, and environmental protection standards.
- Made in Australia: Indicates that the product was manufactured in Australia.
- 0123: The meaning of this code cannot be determined from the images.
Screen Analysis
There is a screen on the front panel of the device, but it is off or blank in the images. Therefore, no analysis of any text, warnings, menus, or values on the screen could be performed.
Dimensions and Compatibility
There is no concrete information regarding the dimensions, size, or user compatibility of the device or accessories in the images. However, given that it is a portable respiratory device and is provided with a carrying case, it is understood to have compact dimensions.
Year of Manufacture
There is no direct information regarding the year of manufacture on the labels. However, the “0123” code on the rear label may be used by some manufacturers to indicate the production date. Whether this code definitively indicates the year of manufacture cannot be determined from the images. The overall design and label format of the device suggest that it is a modern medical device.
Documents
A user manual or information document titled “Information Guide” is visible in the images. This document contains important information regarding the setup, usage, indications, contraindications, and potential side effects of the device. Technical details such as SD card usage are also mentioned. These documents are critical for the buyer to use the device correctly and safely.
Usage Duration
Since the device’s screen is off, no information regarding usage hours or duration was detected in the images. No such information was found on the labels or in the documents.
Existing Faults
There is no evidence of any obvious faults such as broken parts, error messages, frayed cables, or missing components anywhere on the device in the images. The physical condition of the device appears to be good.
Potential Fault Risk
The general condition of the device is good. No concrete signs that could pose a potential fault risk, such as severe wear, rust, or crushed cables, were observed in the images.
