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: 30.09.2026
Report code: 1790769850
NEFES Ventisense PRO Mechanical Ventilator Analysis Report
Device Identification and Basic Information
The product examined in the images is a mechanical ventilator device designed to provide respiratory support. According to the label information on the product, the brand is identified as NEFES and the model as Ventisense PRO. The device body generally consists of a white plastic casing, with a large screen and control panel located on the front surface.
Authenticity and General Condition
The technical labels on the product, the CE 2696 conformity mark, QR code, barcode, and standard symbols have been examined in detail. The quality of all these typographic and visual elements indicates that the product is an original medical device. The general condition of the device is new, and the outer surface is covered with protective stretch film.
Usage Areas
This mechanical ventilator is used in clinical settings or home care processes for the treatment of patients experiencing respiratory failure or those in need of respiratory support. It is preferred in intensive care units and medical situations requiring respiratory support to regulate and monitor the patient’s respiratory parameters.
Quantity Information
The examination of the images shows a total of 1 NEFES Ventisense PRO mechanical ventilator device and 2 orange-colored connection ports/connectors located on the side of the device. No other additional products, parts, or accessories are present in the image.
Physical Deformation and Mechanical Components
When the outer casing and plastic components of the device are examined, no fractures, dents, cracks, or discoloration have been observed on the body. The carrying handle is located on the top and is mechanically sound. There is no deformation or obstruction in the orange-colored port entries on the side panel.
Electronic Components and Screen Analysis
There is a large screen area on the front surface of the device, but the screen is off at the time of inspection; therefore, no menus, values, or warning texts are visible on the screen. Status indicator LED lamps and button icons are located on the upper control panel.
Battery Status
According to the technical information on the rear label of the device, an internal battery is present. The label contains the inscription Li-Ion 18.5V 32Wh; this value indicates the capacity of the battery. As far as can be understood from the image, there is no swelling or liquid leakage protruding from the battery casing.
Label and Text Inventory
All texts and codes on the label on the rear panel of the device are as follows:
- NEFES
- MECHANICAL VENTILATOR
- MODEL: Ventisense PRO
- Made in Turkey
- O2 IN: 25 L/min 1 Bar Max
- Li-Ion 18.5V 32Wh
- AC IN: 100-240V 50/60Hz
- DC IN: 24V
- Max: 60W
- REF: Ventisense PRO
- SN: VP08260351
- MD
- (01)08684190120087
- (11)260217
- (21)VP08260351
- NEFES MEDİKAL TEKNOLOJİ SAN.TİC.LTD.ŞTİ
- Cihangir Mah. Kemal Türkler Sok. No:5/1A Avcılar / İSTANBUL / TURKEY
- CE 2696
- IP22 protection class code
- Standard symbols (refer to user manual, double insulation, medical device symbol, do not dispose of as household waste sign)
The AC IN and DC IN values on the label indicate the electrical supply ranges of the device, the IP22 code indicates the degree of protection against solid objects and water, and the CE 2696 mark indicates compliance with European Union health and safety standards.
Accessories and Connection Ports
There are 2 orange-colored connectors and connection slots on the side panel of the device. There is no external power cable, patient circuit hose, or carrying case in the images. The socket entries are clean and maintain their form.
Dimensions and Compatibility
There is no numerical measurement regarding the dimensions of the product or user compatibility on the labels in the image. The structure of the device is designed to be compatible with standard medical respiratory circuits.
Year of Manufacture
There is no explicit year of manufacture written on the label. However, considering the numerical findings in the VP08260351 code on the SN (Serial Number) line and the data under the (11)260217 barcode, as well as the current label design, it is understood that the device belongs to a recent period. The exact year of manufacture could not be read directly from the texts in the image.
Documents and Usage Duration
There are no invoices, warranty certificates, user manuals, or any printed documents in the images. There is no counter information on the device label or screen showing the total operating hours.
Existing Faults and Potential Risk of Failure
There is no evidence of an existing fault such as a broken part, severed cable, error message, or physical damage on the device in the images. Since the outer surface of the device is protected with stretch film, no risk of serious wear, corrosion, or cable crushing has been observed; it is in good condition.
