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: 20.11.2025
Dräger Vapor 3000 Sevoflurane Anesthesia Vaporizer Analysis Report
Device Identification and Description
The product examined in the visuals is a medical gas anesthesia vaporizer device. The design of the device, its color codes (yellow), and label information confirm that it is a specialized module integrated with modern anesthesia workstations. The device is designed to convert anesthetic agents from liquid to gas form and deliver them to the patient’s breathing circuit at a precise concentration.
Brand and Model Information
As a result of detailed examination of the logos and type labels in the visuals, the manufacturer and brand-model information of the product have been 100% definitively identified as follows:
- Brand: Dräger
- Model: Vapor 3000
- Anesthetic Agent Type: Sevoflurane (Clearly indicated on the device with a yellow color code and text)
Additionally, the front face of the device features the phrase “Provided by Baxter”; however, the rear label clearly states the manufacturer as “Dräger Medical GmbH”.
General Condition and Cosmetic Examination
The device generally appears to be in a well-preserved and ready-to-use condition. Its outer casing is largely clean, but closer inspection reveals the following details:
- Physical Deformation: Superficial scuff marks and slight dirt are present on the white plastic front housing of the device, particularly near the right side of the logo (prominent in image 2). Apart from this, no deep cracks, dents, or broken parts are observed on the casing.
- Color Condition: The yellow top cover and filling cap, characteristic of Sevoflurane, retain their vibrancy; no significant fading has been observed.
- Quantity Information: A total of 1 vaporizer module is present in the visuals.
Technical Label Data and Production Details
The data on the technical label (image 3) located at the rear of the device is legible and provides definitive information about the product’s identity:
- Serial Number (SN): ASKF-0429
- REF (Reference) Code: M36500
- RI Code: 18
- Production Date: 2017-06-15 (Clearly stated as the production date on the label)
- Weight: Indicated by the 8kg symbol.
- Place of Manufacture: Made in Germany
- Manufacturer: Dräger Medical GmbH
Additionally, a separate distribution/tracking label containing the barcode number “01110303FR0004” is located on the side of the device.
Mechanical Components and Functional Controls
During visual inspection, the condition of the device’s mechanical components is as follows:
- Control Dial: The gray rotary dial on the top is in the “0” (closed/locked) position. The “T” (Transport) and level indicators (numbers from 0.2 to 8) are intact and legible. The push button and mechanism on the dial appear sturdy.
- Filling System: The “Dräger Fill” filling system is present at the front-bottom of the device. The filling port and the adjacent liquid level indicator glass appear undamaged. The black tether holding the filling cap is intact and not broken; the cap is not attached but is present as an accessory.
- Locking Mechanism: The gray locking lever (Image 5) located at the rear-top of the device, which secures it to the anesthesia machine (backbar), is in place and robust.
Authenticity and Compatibility Assessment
The device’s labeling standards, material quality, DataMatrix QR codes, and CE certification marks (CE 0123) indicate that the product is an entirely original Dräger item. This unit is designed for use with compatible Dräger-branded anesthesia workstations (e.g., Fabius, Primus, Perseus, etc. series).
Potential Risk and Deficiency Analysis
No significant signs of malfunction (such as broken glass, damaged connection port, or missing dial) that would prevent the device from performing its function are observed. Only the cosmetic scuff marks on the front surface indicate prior use, but this condition does not directly affect the device’s mechanical or pneumatic performance. Since a warranty certificate or invoice is not present in the visuals, the current warranty status is unknown; however, as it was manufactured in 2017, the factory warranty has likely expired.
