Secondhand Philips Respironics Remstar Auto A-Flex AUTOCPAP Device

Objective AI Report

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Report date: 12.02.2026

Philips Respironics REMstar Auto A-Flex (System One) Analysis Report

Device Identification

The main product examined in the visuals is a positive airway pressure (PAP) device used in the treatment of sleep apnea. Alongside the product, a power supply (adapter) and a hose connection are also present.

Brand and Model

As a result of the analyses on the visual, the device’s brand has been definitively identified as Philips Respironics. On the front of the device, just below the screen, the model name is stated as REMstar Auto, and immediately to its right, it is written that this model features A-Flex. The embossed text on the bottom part of the device includes the inscription SYSTEM ONE. In light of this information, the product is the REMstar Auto A-Flex model from the Philips Respironics System One series.

Areas of Use

This device is designed for use in the treatment of obstructive sleep apnea (OSA). The “Auto” designation indicates that the device is an APAP (Automatic Positive Airway Pressure) device capable of automatic pressure adjustment. It automatically increases or decreases air pressure according to the patient’s breathing needs. It is suitable for use in home care settings and sleep laboratories.

Quantity Information

The total number of parts identified in the visual is as follows:

• 1 main device unit.
• 1 power adapter (power supply).
• 1 power cable (connected to the adapter).
• 1 hose (partially visible).

General Condition

The device appears to be in a second-hand and used condition in the visual. The accumulation of dust and dirt on it, particularly around the control knob, indicates that the device has been stored for some time or was in a dusty environment during active use. As it is on surfaces that come into contact with the ground, storage conditions may need to be improved.

Originality

The “Philips Respironics” logo on the product’s casing, the “System One” embossing, screen placement, and font types are fully consistent with original manufacturer standards. The power adapter visible next to it also bears a Philips Respironics brand label, giving the impression of an original accessory.

Physical Deformation and Cosmetic Condition

No deep cracks, breaks, or major dents have been detected on the device’s outer casing. However, cosmetic surface dirt is present. Dust accumulation has been observed between the buttons and in the case’s joint areas. There may be minor signs of wear from use near the upper right corner of the casing and on the front panel, but no damage that compromises structural integrity is visible.

Mechanical Components

The round control knob on the front of the device and the ramp button with the triangular symbol immediately to its right are in place. The physical integrity of these buttons appears sound. The hose connection attached to the right side of the device is physically present.

Accessories and Battery Status

A large, black power adapter is present with the device in the visual. The adapter has a code similar to Ref 1091398 (identified from the readable part) and technical specification labels. The device does not have an internal battery; it requires this external power adapter to operate. Additionally, a white spiral hose (CPAP hose) emerging from the right side is present in the visual, but the entire hose and mask are not visible.

Label Information

Upon examining the label on the power adapter, the following information is readable:

• Brand: Philips Respironics symbols.
• Place of Manufacture: “Made in China” inscription.
• Certifications: CE, UL, IPX1 (water drip protection class) symbols.
• Headquarters Address: Murrysville, PA, USA address details.
• Barcode and Codes: Serial number and part number fields are present on the barcoded label, but the full number cannot be read due to the viewing angle.

Screen Analysis

A monochrome LCD screen is located in the upper middle part of the device. At the time the photo was taken, the device was off or not connected to a power source, so the screen is blank (black). No cracks or stains on the screen were detected from the visual.

Potential Fault Risk and Maintenance Notes

The most prominent risk observed in the device is that of hygiene and filter blockage. The dust on the surface suggests that the air intake filters may also be dirty. As it is a respiratory device, it may require detailed sterilization, internal cleaning, and filter replacement before being put back into use. Other than this, there is no visual evidence of it being electronically or mechanically “broken/damaged.” The device’s condition can be evaluated as a “used product requiring maintenance.”