Secondhand Respirox G3 Luna B30VT BPAP ST Device with Humidifier

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: 12.03.2026
Report code: 1773299167

Respirox G3 B30VT BPAP Device Analysis Report

Device Identification and Areas of Use

The product shown in the images is a BPAP (Bi-level Positive Airway Pressure) device used in the treatment of respiratory tract disorders such as respiratory failure or sleep apnea. It provides respiratory support to the patient by applying positive airway pressure at two different levels via a mask. It is suitable for home use and clinical environments.

Brand and Model Information

The brand of the device has been identified as Respirox, and its model as G3 B30VT. This information has been verified from the logo on the front panel of the device and the manufacturer’s label on the rear.

Authenticity Assessment

Upon examining details such as the device’s casing craftsmanship, screen resolution, menu interface, label print quality, and branded carrying case, the product is assessed to be original.

Quantity and Accessory Information

The product and accessories identified in the images are as follows:

• 1 Respirox BPAP main device
• 1 integrated humidifier unit
• 1 grey respiratory hose
• 1 full-face respiratory mask with headgear
• 1 power adapter and cable
• 1 grey carrying bag with shoulder strap

General Condition and Physical State

The device is used, and its general condition is very good. There are no scratches, cracks, breaks, dents, or discoloration on the casing, screen, or the transparent humidifier chamber. The device and its accessories are clean.

Mechanical and Electronic Components

The power button on the top of the device and the rotary adjustment knob on the front panel are physically intact. The blue LED illumination of the power button is functional. The color LCD screen displays images without any issues. There are no dead pixels, lines, or darkening on the screen. The connection points of the humidifier chamber to the device and the hose input sockets are robust.

Screen and Interface Analysis

When the device is operational, real-time respiratory data is monitored on the screen. The parameters displayed on the screen are as follows:

• Pressure Instantaneous applied air pressure (seen as 3.7 cmH2O and 6.4 cmH2O in the images).
• Vt Tidal volume value (in mL).
• Leak Amount of air leakage in the mask or hose (in L/min).

At the bottom of the screen, there are menu tabs for “Real-time data”, “Real-time waveform”, “Current Settings”, and “Settings”.

Label and Technical Information

The information on the label located at the rear of the device is as follows:

• Device Type BPAP System
• Model Code G3 B30VT
• SUT Code DO1014
• UDI Barcode Number (01)06948538365458
• Production Date Code (11)230924
• Serial Number (21)B3CBC904137

Additionally, there is a warning label on the humidifier chamber. This label states the warning: “CAUTION!!! ABSOLUTELY DO NOT CARRY THE HUMIDIFIER UNIT WHEN IT CONTAINS WATER. OTHERWISE, YOUR DEVICE WILL BE OUT OF WARRANTY.”

Year of Manufacture

According to the (11) barcode identifier standards on the device’s rear label, the manufacturing date has been determined as September 24, 2023.

Dimensions and Compatibility

The device is of standard desktop dimensions. The accompanying mask and headgear are compatible with adult patients in terms of size.

Existing Faults and Potential Risks

No broken parts, error messages, or existing faults related to the device have been detected in the images. The device’s condition is good. There is only a risk of water leaking into the electronic components if the device is moved while the humidifier chamber contains water. Other than this, no observed fault risks exist.