Secondhand PAP Humidifier Philips Respironics Remstar 1056216

Objective AI Report

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Report date: 21.02.2026

Respironics System One REMstar Heated Humidifier Analysis Report

Device Identification and Areas of Use

The product submitted for examination is a medical accessory and sub-component device used by integration into respiratory devices (CPAP or BPAP systems). From the form structure in the visuals and the label declarations underneath, it has been determined that the device is a heated humidifier unit (Heated Humidifier) developed for the purpose of humidifying the air supplied to the device. It has been manufactured for use in increasing breathing comfort by connecting to the main respiratory device in the treatment of respiratory ailments such as sleep apnea.

Brand and Model Identification

Upon detailed examination of the visuals, the inscription SYSTEM ONE is embossed in plastic relief on the product casing. Based on evidence obtained from the metallic information label at the base of the device, the product brand has been identified as Respironics, and the model as REMstar Heated Humid., INTL. The device is an original sub-module of Respironics’ System One respiratory therapy series.

Originality Status

The label structure indicating safety and compliance standards (CE, ETL Listed) on the underside of the product, the serial/name inscriptions pressed into the casing, and the matte and uniform texture of the plastic raw material used point to professional standards. Considering both the technical serial number coding and the medical certificate warnings, it is understood that the part presented is a completely original part meeting manufacturer standards.

General Condition and Status

As a result of visual analysis, the humidifier module generally appears clean. Although it is understood that it is not a completely new device, it has been generally maintained and kept clean. No significant fading in the product color or loosening in the materials is observed, and the device successfully maintains its form.

Physical Deformation Examination

No evidence of impact, dents, or deep scratches was found on the side and rear plastic surfaces of the casing. The only notable deformation detail in the physical external observation was observed on the paper instruction label, which expresses usage instructions with symbols, on the top platform of the product. The corner of the label and its connection area have lifted and slightly lost their form, but this does not affect the device’s performance. The left transparent section is free from dirt or cloudiness, and there is no plastic fatigue affecting functionality.

Mechanical Component Examination

The infrastructure slide designed to clamp the device to the main unit, and the movable upper tube/socket part (black cylindrical protruding hose port) that connects to the respiratory set or hose group, appear physically sound and complete. No signs of breakage or deformation were detected in the locking tabs.

Electronics and Port Analysis

The device is in the form of an external cabinet; the photos show the external chassis structure rather than a direct electronic data output. It does not have mechanisms such as an independent battery, battery-powered input, or a display screen; instead, since it draws all control connections directly mechanically from the CPAP device it is attached to, no parts are found that would pose a risk of faulty electronic data transfer specific to the product.

Quantity Information and Accessories

Within the scope of this report, only 1 unit of the humidifier platform’s lower and outer body (lower body assembled and in a complete set form) is listed. A standard-sized transparent connection port is attached to the product to ensure air transmission during use. The power compressor motor unit providing respiratory therapy, filters, or external electrical cable, air and carrying tubes are not visualized within the set in the report.

Label and Technical Values

The products have a dual base label containing both English written device warnings and quality seals.

• Product Description: REMstar Heated Humid., INTL
• REF Code (Device Base): 1056216
• Bottom Barcode Coding: E3BA Rev. 00
• Sealing Norm: IPX1 (Standard insulation protected against dripping water)
• Instruction Sticker Reference No (On the top-located part): REF 1062836
• Medical Classification and Descriptions: This is a medical device. European medical approval and 0123 CE standard compliance, warning logo standards are processed.

Size, Structure, and Production Period Clues

Visually, it has a standard sleep/CPAP equipment structure; it confirms that it can be used based on clinical decision for respiratory ailments, but its dimensions indicate that it belongs to square-designed home/room systems that ergonomically fit at the head of the bed. Since there is no clear printed current year serial/day stamp on the top paper covering the instructions or in the production reference information, a precise estimation could not be made.

Notification of Potential Malfunction Risk

The critical importance of such humidifier chambers is that no blockage or cracking is observed between the ports; when its structure is checked, no signs of leakage or port damage are seen. Since the product maintains its completely solid form and smooth lower slots, it does not pose a risk and exhibits very good integrity, reflecting the prediction of seamless connection.