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: 22.09.2026
Report code: 1790062940
SALVIA LIFETEC ALPHA 101c Device Analysis Report
Device Identification and Credentials
The examined images feature a medical device, model ALPHA 101c, from the brand SALVIA LIFETEC. The SALVIA LIFETEC inscription and the ALPHA 101c model code are clearly legible on the front panel.
- Device Type: Medical respiratory and ventilation support device.
- Brand: SALVIA LIFETEC
- Model: ALPHA 101c
Authenticity and General Condition
The device appears to be original when examining the outer casing, technical drawings on the front panel, inscriptions, and the craftsmanship quality of the control knobs. The device is generally clean and in good condition.
- General Condition: Used but well-maintained and clean.
- Physical Deformation: There are no breaks, cracks, dents, or deep scratches on the casing surface or the front panel. There is a blue-toned label residue or trace on the left side of the front panel.
Usage Areas
This device is designed for use in clinical settings and intensive care units to monitor patients’ respiratory parameters and provide respiratory support.
Quantity Information
The total number of products and accessories in the images has been examined:
- Main Device: 1 unit of SALVIA LIFETEC ALPHA 101c main body.
- Accessories: 1 black-colored hose, 1 white-colored hose with a metal tip.
Mechanical and Electronic Components
Mechanical and electronic components have been evaluated based on the images:
- Mechanical Components: The adjustment knobs (potentiometers) on the front panel are in place and appear mechanically sound. There are no blockages or damage to the ventilation grilles on the rear panel of the device.
- Electronic Components: An integrated electronic screen is located on the front panel, with parameter adjustment knobs situated below it. An on/off switch is present on the rear panel.
Accessories and Connection Points
There are two hose accessories connected to the device:
- Black Hose: A flexible black connection hose attached to the rear of the device.
- White Hose: A flexible white connection hose with a metal-tipped connector.
- Sockets and Inputs: Metal connection ports and a black main output port are located on the lower left side of the front panel. The power input and fuse housing are located on the rear panel.
- Expiration Date: There is no information regarding an expiration date on the accessories.
Battery Status
There is no external visual evidence or label information regarding the device’s internal battery or an external battery unit in the images.
Label and Inscription Inventory
Inscriptions and labels located on the device body have been identified in the images:
- Front Panel Inscriptions: ALPHA 101c, SALVIA LIFETEC, Ausatemventil, Vernebler, Einschalt-Druck, Trigger, Fluß 1/min., Sauerstoff Konzentration %, Verneblerleistung, Ausatemwiderstand, Ausschalt-Druck, Atemwegsdruck [mbar], Zeit [min], AF [1/min].
- Service Label: The label on the front panel contains information for SESAN, 0(232) 483 50 51, and www.sesanltd.com.tr. This information indicates that the authorized or relevant medical service provider can be contacted.
- Rear Panel Inscriptions: AUS / OFF / ARRETMARCHE, EIN / ON / MARCHE, 500 mAT, Type: FST. The 500 mAT inscription indicates the fuse current rating of the device.
Screen Analysis
A digital screen is located in the upper middle part of the front panel. Since the device is turned off or the screen is inactive in the images, no text, values, or warnings are visible on the screen.
Dimensions and Compatibility
There is no numerical dimension information regarding the physical measurements of the device or user compatibility in the images.
Year of Manufacture
There is no clear year of manufacture information on the labels or surfaces in the images. Given the design lines and label style of the device, it is understood to be a professional-grade medical device from a specific period; however, a precise year of manufacture could not be determined due to the lack of concrete data.
Documents
There are no written documents such as invoices, warranty certificates, user manuals, or similar items in the images.
Usage Duration
As the device screen is off and there is no counter data on the labels indicating operating hours, there is no information regarding the usage duration in the images.
Existing Faults
There is no clear evidence of faults such as a broken casing, error codes on the screen, severed cables, or missing main parts in the images.
Potential Risk of Fault
Except for the blue label residue on the front panel, no concrete risks such as severe wear, rust, or crushing on the cables have been observed. The general condition is good.
