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: 09.06.2026
Report code: 1781010068
PHILIPS PRACTIX 33 plus Mobile X-Ray System Analysis Report
Device Identification and Brand Model Information
In the images, a mobile X-ray system containing a movable arm and an X-ray tube on a wheeled base has been identified. The labels located on the main unit of the device and the X-ray tube have been examined in detail.
- Device Brand-Model: PHILIPS PRACTIX 33 plus
- Tank Unit Brand-Model: TECHNIX MHF 833
- X-Ray Tube Brand-Model: TECHNIX DF-151SB-T
Authenticity Assessment
Considering the PHILIPS and TECHNIX logos on the device, the print quality of the labels, and the general workmanship details, the product is assessed to be original.
Usage Areas
This mobile X-ray system is used for diagnostic imaging purposes in hospitals, clinics, emergency departments, intensive care units, and plaster rooms. It is an important tool for diagnosing bone and joint injuries and abnormalities.
Quantity Information
The images contain one mobile X-ray system and its integrated accessories.
General Condition and Physical Deformation
The general condition of the device is assessed as used. No significant scratches, dents, or cracks have been observed on the casing. There is no color fading or heavy dirt/dust accumulation.
Mechanical and Electronic Component Inspection
No visible issues have been detected in the mechanical components such as the wheels, the movable arm mechanism, and the handles. Electronic components such as the X-ray tube and the control panel on the main unit appear visually intact. The cables are neatly organized.
Accessories
The device has an integrated power cable and X-ray tube connection cables. No external box or additional accessories are present in the image. Socket inputs are not clearly visible in the image.
Battery Status
There is no internal or external battery or any indicator providing information about the battery status in the images.
Label Information
There are two main labels on the device:
- PHILIPS Label (Main Unit):
- Brand: PHILIPS
- Model: PRACTIX 33 plus
- Type: Mobile Medical X-ray System – Indicates that the device is a mobile X-ray imaging system.
- Serial Number: P5-679 – The unique identification number of the device.
- Input: 230/115 V~, 1 Phase, 50/60 Hz, 16 A, 34 A – Shows the electrical power requirements (voltage, phase, frequency, and current) of the device.
- Date Mfg: MAY 2006 – Indicates the month and year of manufacture of the device.
- Classification: Class I – TYPE B, IEC 60601-1, Assembled Equipment IEC 60601-2-32-1994 – Shows the electrical safety classification of the device and its compliance with relevant international standards.
- CE Mark: CE 0123 – Indicates that the product complies with European Union health, safety, and environmental protection standards and specifies the notified body number.
- Place of Manufacture: Made in Italy – Indicates the country where the device was manufactured.
- TECHNIX Label (X-Ray Tube Unit):
- Brand: TECHNIX S.p.A.
- Tank Unit: MHF 833 – The model of the tank unit containing the X-ray tube.
- Serial Number (Tank Unit): 1761 – The unique identification number of the tank unit.
- X-Ray Tube: DF-151SB-T – The model of the X-ray tube.
- Serial Number (X-Ray Tube): 6K1744 – The unique identification number of the X-ray tube.
- U: 110 kVp max – Indicates the maximum peak voltage (kilovolt peak) of the X-ray tube.
- I: 80 mA – Indicates the maximum current (milliampere) of the X-ray tube.
- Permanent filtration: 1,5 IEC 60336, 0,7 Al/75kV – Indicates the permanent filtration values of the X-ray beam and the relevant standard.
- CE Mark: CE 0051 – Indicates that the product complies with European Union health, safety, and environmental protection standards and specifies the notified body number.
- Place of Manufacture: Made in Italy – Indicates the country where the X-ray tube unit was manufactured.
Screen Analysis
No screen is visible on the device or it is in an off state. Therefore, the text or values on the screen could not be analyzed.
Dimensions and Compatibility
There is no direct information regarding the dimensions of the device or user compatibility in the images. However, its wheeled structure and design, typical for mobile X-ray systems, indicate that the device can be easily moved in different hospital environments and can adapt to various patient positions.
Year of Manufacture
The information “Date Mfg: MAY 2006” is clearly stated on the PHILIPS label. According to this information, the year of manufacture of the device is 2006.
Documents
There are no documents such as invoices, warranty certificates, or user manuals belonging to the device in the images.
Usage Duration
No information regarding the operating hours or total usage duration could be detected on the screen, label, or any document of the device.
Existing Fault
No clear evidence of a fault such as a broken part, error message, disconnected cable, or missing component has been observed in the images.
Potential Fault Risk
The general condition of the device is good. No concrete situation that could pose a potential fault risk, such as severe wear, rusting, or cable crushing, has been detected in the images.
