Secondhand PAP Humidifier Philips Respironics Remstar 1056216

Objective AI Report

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Report date: 23.02.2026

Respironics System One REMstar Heated Humidifier Analysis Report

Device Identification

The product examined in the visuals is an active humidification module designed to be integrated into respiratory devices (CPAP/BiPAP). The product is not an independent treatment device, but “Heated Humidifier” equipment that connects to System One series devices.

Brand and Model

Brand: Respironics (According to label information Respironics Inc. / Respironics Deutschland)
Product Family: System One (Embossed on the casing)
Device Description: REMstar Heated Humid, INTL (Bottom label information)
Model/Reference Number (REF): 1056216

Areas of Use and Compatibility

This equipment is compatible with Respironics System One series CPAP and BiPAP devices used in the treatment of Sleep Apnea or respiratory failure. The device aims to increase patient comfort and prevent dryness in the upper respiratory tract by heating and humidifying the therapy air.

Originality and Manufacturer Information

The labels, font quality, embossed logos, and serial number barcodes on the product confirm that it is an original Respironics product. The manufacturer’s address is stated as “1001 Murry Ridge Lane, Murrysville, PA 15668 USA”.

General Condition and Physical State

During visual inspection, the device appears used but in clean condition. The casing integrity is preserved, and no deep cracks or fractures have been detected. It is assessed that there may be slight superficial marks on the black plastic surfaces due to normal use, but no noticeable heavy damage is present.

Mechanical and Accessory Analysis

• Casing: The black hard plastic body is robust. The side latch and connection points appear regular.
• Top Lid and Port: In the middle of the top lid, there is a steerable transparent air outlet port for hose connection. No damage has been observed in the externally visible hinge structure of the lid’s opening and closing mechanism.
• Heater Plate Area: In the front part of the device, there is a grey-colored area, presumed to have a sealing gasket. The slot where the water chamber is placed appears clean.
• Water Chamber: It is not clearly distinguishable in the visuals whether a transparent water chamber is installed inside the device. However, the front cover/wall structure is in a closed position. A transparent water tank is not presented separately as an external spare part in the visual; only the main unit is being reported.

Label and Technical Information

The following technical data has been collected from the labels located on the bottom and top of the device:

• Main REF Code: 1056216 (The actual reference code on the base of the device)
• Top Lid Code: REF 1062836 (Part code found on the instruction label on the top lid)
• Protection Class: IPX1 (Protected against dripping water)
• Certification: CE 0123 certified, CSA US approved. The phrase “This is a medical device” is present.
• Lot/Serial Information: Although serial number barcodes and production date codes are present on the label, the full serial number (SN) cannot be read due to the photographic angle. A production code such as “E30A” or similar is partially visible.

User Interface and Information

On the top lid of the device, a 5-step pictorial user guide sticker is affixed, showing how the user can remove, install, and fill the water chamber. The label is in good condition and fully legible.

Connection Interface

In the rear bottom part of the device (the side that connects to the CPAP device), metallic pin connectors providing electrical transmission and data exchange, and an air passage channel opening are visible. The connector slot appears clean.

Quantity Information

The visuals show 1 (one) unit of Respironics System One Heated Humidifier. An external power adapter, connecting hose, or box contents are not visible.

Potential Omissions and Notes

The Respironics System One series main device (Blower/Motor unit) and power supply, which are necessary for the device to operate, are not included in the visuals. This product cannot be operated independently; it is a complementary part of a compatible main device. The condition of the water chamber could not be verified due to the closed lid.