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: 10.06.2026
Report code: 1781081386
EASYPOD Injection Device and Accessories Analysis Report
Device Identification and Brand Model Information
The images show a portable injection device, a carrying/storage case that appears to belong to this device, and an additional component. The EASYPOD brand is clearly visible on the device and its label. The label on the bottom of the device contains the code REF: AZ1M4-00252-1-1. This code indicates the reference number of the product.
Authenticity Assessment
When examining the logo quality on the device, the clarity of the labels, and the general workmanship details, the impression is that the product is authentic. The CE mark and other symbols on the label indicate that the product complies with certain standards.
Usage Areas
The EASYPOD device in the image is a portable injection device. Such devices are generally used by patients for self-administration of specific medications, particularly in treatments requiring regular and precise dosage, such as growth hormone. The design of the device is suitable for easy use at home or while traveling.
Quantity Information
- Main Device (EASYPOD Injection Device): 1 unit
- Carrying/Storage Case: 1 unit
- Additional Component (White and blue colored, with EASYPOD logo): 1 unit
- Small, sealed containers (likely medication cartridges): 4 units
General Condition and Physical Deformation
The general condition of the device is considered used. There is slight dirt and discoloration on the white and blue casing of the device. Yellowing due to use is observed, especially on the white surfaces. There are no scratches or cracks on the screen of the device, but the screen is in the off state. The additional component also shows similar slight dirt and discoloration.
Mechanical and Electronic Components
There are three buttons on the front of the device. These buttons appear to be physically intact. There is a transparent section on the side of the device that appears to be a cartridge or medication chamber. There is a dark-colored cartridge inside this section. No visible breaks or cracks have been detected in the mechanical components. The status of the electronic components cannot be visually assessed due to the device being powered off.
Accessories
The device is presented in a specially designed blue carrying/storage case. Inside the case, in addition to the device, there are four small, sealed containers. These containers are estimated to be medication cartridges. There are no socket inputs or cables visible on the device. The expiration dates of the accessories are not clearly readable in the images.
Battery Status
There is no clear information in the images regarding the status of the internal or external battery. The battery compartment or the battery itself is not visible.
Label Information
- Serial Number: 3M 511 21004084
- REF Code: AZ1M4-00252-1-1
- Manufacturer Information: Merck Trading S.A., an affiliate of Merck KGaA, Darmstadt, Germany
- Year of Manufacture: 2013
- CE Mark: Indicates that the device complies with European Union health, safety, and environmental protection standards.
- Crossed-Out Wheeled Bin Symbol: Indicates that waste electrical and electronic equipment must be collected separately.
- Manufacturer Symbol: Symbol indicating the manufacturer.
- Consult Instructions for Use Symbol: Indicates that the user must read the user manual before using the device.
Serial Number (Ser. No: 3M 511 21004084): This number is an identification code that uniquely identifies each device. It is used for product tracking, warranty processes, and service operations.
REF Code (REF: AZ1M4-00252-1-1): This code is the reference number that identifies a specific model or configuration of the product. This code is used when ordering spare parts or receiving technical support.
Manufacturer Information (Merck Trading S.A., an affiliate of Merck KGaA, Darmstadt, Germany): This information indicates the manufacturer and origin of the device. It is an important reference regarding the quality and reliability of the product.
Year of Manufacture (2013): Indicates the year the device was manufactured. This information provides an idea about the age and potential service life of the device.
Screen Analysis
The device’s screen is in the off state. Therefore, no analysis of any text, warning, menu, or value on the screen can be performed.
Size and Compatibility
There is no clear information in the images regarding the dimensions or size of the device. However, it is understood from visual cues that the device is of a size that can be easily held in one hand and has a portable and compact design. This indicates that the device is suitable for personal use.
Year of Manufacture
The year of manufacture is clearly stated as 2013 on the label at the bottom of the device.
Documents
No documents such as invoices, warranty certificates, or user manuals belonging to the device are visible in the images.
Usage Duration
There is no information regarding usage hours or total usage duration on the device’s screen, label, or any document in the images.
Existing Fault
No clear evidence of a fault, such as a broken part, error message, or severed cable that would prevent the device from working, has been detected in the images. The general physical condition of the device does not show signs of a major fault, other than wear and tear due to use.
Potential Fault Risk
Apart from the slight discoloration and dirt observed on the casing of the device, no tangible wear that would pose a serious potential fault risk, such as rusting or cable crushing, has been detected. The general condition of the device is at an acceptable level for its age.
