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: 15.05.2026
Report code: 1778844061
Covidien Kendall SCD 700 Series Compression Device Analysis Report
Device Identification
The main product in the images is a pneumatic compression device used for deep vein thrombosis (DVT) prophylaxis. Numerous disposable compression sleeves and connection hoses are visible along with the device.
Brand and Model
Following an examination of the front panel and labels, the brand and model information have been clearly identified. The brand of the device is Covidien, and the model is Kendall SCD 700 Series. The brands Cardinal Health and Kendall are visible on the sleeves.
Authenticity
The print quality of the logos on the device, the layout of the labels, the serial number and barcode information, the craftsmanship of the plastic casing, and the structure of the screen indicate an original product. The packaging and technical information on the sleeves also possess the characteristics of original medical supplies.
Usage Areas
This device is used in hospitals or at home for bedridden patients, in the post-operative period, or in cases of limited mobility to prevent the formation of blood clots (deep vein thrombosis) in the legs. The device accelerates blood circulation by sequentially inflating and deflating the sleeves wrapped around the legs. It is suitable for use in branches such as general surgery, orthopedics, neurology, and intensive care. The sleeves in the image are compatible consumables for this device.
Quantity Information
There is 1 Covidien Kendall SCD 700 Series compression device in the images. 1 power cable is visible wrapped around the back of the device. Additionally, there are 2 transparent connection hoses in transparent bags. A large number (approximately 10-12 units) of compression sleeves in various sizes (S, L, M) have been identified in their packaging.
General Condition
The general condition of the device appears to be very good and clean. There is no significant wear, discoloration, or dirt on the plastic casing. Most of the sleeves are in their original, unopened packaging. The impression is that the device has been lightly used or very well maintained.
Physical Deformation
No scratches, cracks, dents, or broken parts have been observed on the front panel, screen, or rear casing of the device. The carrying handle is sturdy. A protective film layer is visible on the screen. The sleeve packaging maintains its integrity.
Mechanical Components
The carrying handle, the cable management section at the back, and the hose connection sockets appear to be sturdy. No breakage or loosening has been detected in any mechanical parts. The Velcro sections of the sleeves could not be checked as they are packaged, but the packages are intact.
Electronic Components
The power button, channel A and B buttons, and the screen on the front panel appear to be in good condition. The power cable input socket on the back of the device and the cable itself are undamaged. As the device was not powered on, there is no visual data regarding the functionality of the screen or the status of the internal electronic circuits.
Accessories
There is an integrated power cable at the back of the device. 2 transparent connection hoses are present. There are numerous compression sleeves in various sizes (S, L, M) and types (Thigh Length). REF codes (e.g., 73011, 73012, 73013) and size information are clearly legible on the sleeve packaging. Expiration date information for the sleeves could not be determined from the images.
Battery Status
There is no clear information on the labels or the front panel regarding whether the device has an internal battery. The power cable is wrapped at the back of the device, which indicates that the device primarily operates on mains electricity. No external cover or signs of swelling related to a battery compartment have been observed.
Label Information
The label on the back of the device contains the following information:
- Serial Number: 133100223X
- REF Code: 29525100
- Technical Information: 100-240V ~, 50/60Hz, 200mA
- Manufacturer Information: Covidien LLC, Mansfield, MA
Different REF codes (73011, 73012, 73013) and barcodes are also present on the sleeve packaging.
Screen Analysis
The device screen is in the off position. Therefore, no analysis could be performed regarding the text, menus, or warnings on the screen. The screen surface is clean and undamaged.
Size and Compatibility
The device itself is of a portable size. Size information (S, M, L) and thigh circumference measurements (e.g., <22 in./55.9 cm, 28-36 in./71.1-91.4 cm) are provided on the sleeves. This information indicates the compatibility of the sleeves with different patient sizes.
Year of Manufacture
No clear date information regarding the year of manufacture could be identified on the labels on the device or the sleeve packaging.
Documents
No invoices, warranty certificates, or user manuals belonging to the device are visible in the images.
Usage Duration
There is no information on the screen or labels regarding the total operating hours of the device.
Existing Faults
There is no clear evidence in the images, such as broken parts, burn marks, or error messages, indicating that the device is faulty.
Potential Risk of Failure
The physical condition of the device is very good. No crushing of cables, corrosion on sockets, or significant wear on the casing has been observed. Therefore, based on visual data, it can be said that the device is in good condition and carries a low risk of failure. Since the sleeves are disposable, they do not pose a risk in terms of hygiene.
