Secondhand Carefusion LTV 1200 Transport Mechanical Ventilator

Objective AI Report

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Report date: 04.11.2025

CareFusion LTV 1200 Ventilator Analysis Report

Overview and Device Description

The product shown in the visuals is a ventilator, a medical device used to provide respiratory support. It is clearly stated on the device’s front panel and in the accompanying user manual that the device is a CareFusion brand, LTV 1200 model. The device, by its design and features, is used to support patient respiration in hospitals or home care settings. Judging by the quality of the logo and labels in the visuals, the product appears to be original.

Package Contents and Quantity Information

As a result of the count performed in the visuals, the following items were identified:

• 1 CareFusion LTV 1200 Ventilator Device
• 1 “Operator’s Manual” (User Manual)

Physical Condition and Deformation Analysis

The device generally has a clean and well-maintained appearance, though it is a used product. No significant cracks, breaks, or dents are observed on the dark blue rubber protective parts or the gray main body. There is no noticeable color fading on the surfaces, but very slight superficial marks, possibly due to use, are present. No heavy accumulation of dust or dirt is visible on the device or its ventilation grilles.

Mechanical and Electronic Component Examination

The mechanical and electronic components of the device are visually in good condition. All control knobs and buttons on the front panel are in place and do not appear physically damaged. The rotary adjustment knob also has a sturdy structure. The gas outlet port and other connection points on the side of the device are clean and free from deformation. One visual shows the device’s screen operating and displaying data, indicating that the electronic system is fundamentally functional.

Screen Analysis and Detected Warnings

The device’s screen is operational and displays numerical values for various respiratory parameters. A warning message “DISC/SENS.” is displayed at the top of the screen. This is typically an alarm condition indicating a sensor error or that the patient circuit is not connected to the device. Other parameters read on the screen are:

• Frekvens (Frequency): 20
• Tidalvolum (Tidal Volume): 5.0
• Trykkregulering (Pressure Regulation): 1.5 and 0.3
• Insp. tid (Inspiration Time): 1.0
• PIV (cmH2O/PEEP): 21
• Følsomhet (Sensitivity): 2
• Høyt trykk (High Pressure Alarm): 3.0
• Lavt trykk (Low Pressure Alarm): 1.0
• Lav min. vol. (Low Minute Volume Alarm): 0.5
• PEEP/CPAP: 0

Additionally, the screen features LED indicators showing statuses such as “Pasientaktivitet” (Patient Activity), “Ekst. spenning” (External Voltage), “Lader/lavt” (Charger/Low), and “Batterimodus” (Battery Mode).

Accessories and Connection Ports

A spiral-bound user manual is included with the device. The manual’s cover features the title “LTV 1200, 1150 Ventilator, and MR Conditional LTV 1200 System Operator’s Manual”. Various connection ports are visible on the rear of the device:

• Gas Outlet (Gas Outlet): The main gas outlet port located on the front side.
• O2 Inlet (Oxygen Inlet): The oxygen inlet port with a green protective cap.
• Patient Assist (Patient Assist): A port with a cable connected.
• Comm Port (Communication Port): An RJ-45 type communication port.
• Additionally, a power input and a fan grille are also present on the rear panel.

Labels and Technical Information

In the visuals, a label showing the device’s serial number, REF code, or manufacturing year could not be clearly read. However, various technical details are present on the device:

• Top Panel Label: On the upper part of the device, there is an “LTV Ventilator Quick Reference Guide” label explaining basic functions and alarm interventions.
• Oxygen Inlet Information: Next to the O2 Inlet port, inlet pressure values are specified as “3.5-5.5 BAR OR 50 LPIS 60 PSI MAX”.

Conclusion and Potential Risk Assessment

The CareFusion LTV 1200 ventilator device is in good physical condition despite being used. No serious damage or deformation is observed on the casing, keypad, or connection ports. It is understood from the screen that the device is operational. However, the “DISC/SENS.” warning displayed on the screen indicates that the device was either tested without a patient circuit connected or that there might be a sensor malfunction. This finding highlights the critical need for the device to be checked and calibrated by an authorized technical service before use. Considering the overall physical integrity of the device, no significant potential risk of malfunction is observed apart from the existing warning.