Objective AI Report
Disclaimer: I am Medbidding AI. I am an unbiased AI agent. 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: 11.10.2026
Report code: 1791722980
plusmed pM-KN01 Oxygen Concentrator Analysis Report
Device Identification and Basic Information
The examined device is an oxygen concentrator used in home-type respiratory support therapies. The image displays the main unit along with a humidifier bottle, connection hoses, and an electrical power cable. The brand and model information of the device has been clearly read from the labels on the housing.
Brand and Model
The product brand is determined as plusmed, and the model is identified as pM-KN01 Oxygen Concentrator. This information is located on the logo on the front surface of the housing and on the technical label on the rear panel.
Authenticity Assessment
Upon examining the placement of the brand logos, type labels, and warning texts, it is observed that the device is an original plusmed production.
Usage Areas
This device is used in home environments or clinical settings to provide high-purity medical oxygen by filtering the ambient air for the treatment of patients suffering from respiratory failure or those in need of oxygen support.
Quantity Information
The images show 1 main oxygen concentrator, 1 humidifier bottle, attached transparent oxygen delivery hoses, 1 nasal cannula, and 1 black electrical power cable.
General Condition
The device is in a used condition. There are slight discolorations and surface stains on the plastic outer casing, but its general condition is functional.
Physical Deformation
Traces of use, dust accumulation, and slight friction marks are visible on the outer plastic panels of the housing and the lower gray base section. No cracks or fractures have been detected in the area surrounding the display panel or on the housing surface.
Mechanical Components
The lower part of the device features wheels that provide mobility. The carrying handle on the top, the flow adjustment valve on the front, and the humidifier bottle cradle on the left side are securely in place.
Electronic Components
The top panel features a black keypad and a digital display with blue backlighting. The rear panel contains the power input socket and the power switch.
Accessories
The device comes with transparent connection hoses, a nasal oxygen cannula, a humidifier bottle with water level markings, and a standard black electrical power cable. The socket inputs are in good condition.
Battery Status
The device does not contain an internal or external battery; it operates directly via mains electricity.
Label and Text Inventory
The front surface of the housing contains warning texts in Turkish and English: CAUTION: Please read the user manual before operating the machine. Non-professionals are prohibited from opening the machine’s shell. It is recommended to clean the dust filter once a month and replace the air intake filter once a month. The oxygen purity is 93%±3%. NO SMOKING OR NAKED FLAMES IN THE ENVIRONMENT. DO NOT USE OIL OR GREASE. CAUTION: Please read user manual before operation. Nonprofessional prohibited to open shell of machine. Clean intake air filter every months. Change secondary filter every months. The oxygen purity is 93%±3% while in rated flowrate. NO SMOKING OR NAKED FLAMES. USE NO OIL OR GREASE. The rear label displays the following technical data: Model: pM-KN01 Oxygen Concentrator, Power: 480 W, Oxygen Saturation: 93% ± 3%, Voltage: AC230 ± 10%, 50/60 Hz, Oxygen Flow: 0-5 Lpm, Outlet Pressure: 0.04 – 0.07 Mpa, SN: MZJ5S 43072, CE 1984 mark, and manufacturer information.
Display Analysis
On the blue display on the top panel, there are status LED lamps or indicator labels containing the abbreviations PO, PF, L.P., H.F., L.O2, H.O2; these lamps indicate the operating status of the device and potential pressure or flow warnings.
Dimensions and Compatibility
There is no direct measurement information in the images, but it is understood from the label that the device is of standard home-type wheeled concentrator dimensions and offers a 0-5 Lpm flow capacity.
Year of Manufacture
The year of manufacture is not explicitly written on the label, but the design structure and label format of the device concretely reflect recent medical device standards.
Documents
The images do not include an invoice, warranty certificate, or printed user manual.
Usage Duration
There is no counter information visible on the device’s display or labels indicating the total usage hours.
Existing Faults
There is no clear evidence of a fault such as a broken part, error message on the screen, or a severed cable in the images.
Potential Risk of Failure
Except for superficial stains on the plastic surface of the housing, no serious wear, rust, or cable crushing has been observed; the general condition is clean and tidy.
