What to do if my Weinmann Medical Equipment displays 'Arrange maintenance'?
If your device displays 'Arrange maintenance', it needs to be checked or serviced by Weinmann or a specialist dealer as soon as possible because the maintenance interval has expired.
What to do if the Weinmann Medical Equipment shows a filter change indicator?
If the filter change indicator appears, clean or change the filter as soon as possible.
Why does the 'Change filter' message appear on my Weinmann VENTIlogic LS Medical Equipment?
The 'Change filter' message appears because the filter is dirty. Press the alarm acknowledgement key, and clean or change the filter as soon as possible.
What to do if Weinmann Medical Equipment displays service life ended for internal battery?
If your Weinmann Medical Equipment displays 'Service life ended. Have internal battery replaced', it means the internal battery has reached the end of its service life. Replace the internal battery.
What to do if Weinmann VENTIlogic LS displays service life ended for replaceable battery?
If your Weinmann Medical Equipment displays 'Service life ended. Have replaceable battery replaced', it means the replaceable battery has reached the end of its service life. Replace the replaceable battery.
What does BT low mean on Weinmann Medical Equipment?
If the Weinmann Medical Equipment displays 'BT low', the settings may be implausible. Have the settings checked by the doctor supervising treatment.
How to fix filter change on Weinmann Medical Equipment?
If the Weinmann Medical Equipment indicates a filter change, it's likely because the filter is dirty. You should press the alarm acknowledgement key and clean or change the filter as soon as possible.
What causes blower failure in Weinmann VENTIlogic LS?
If there is a blower failure in your Weinmann Medical Equipment, have the device repaired, because the blower is no longer working.
Why replaceable battery is hard to push in Weinmann Medical Equipment?
If the replaceable battery is hard to push in or jams in your Weinmann Medical Equipment, it's likely due to dust particles in the guide rails. Clean the guide rails on both the replaceable battery and the lower part of the housing.
What does arrange maintenance mean on Weinmann Medical Equipment?
If your Weinmann Medical Equipment indicates that maintenance is required, the device needs to be checked or serviced by Weinmann or a specialist dealer as soon as possible because the maintenance interval has expired.
General| Brand | Weinmann |
|---|---|
| Model | VENTIlogic LS |
| Category | Medical Equipment |
| Language | English |
Explains the numbered components of the therapy device shown in the illustration.
Describes the components of the therapy device used with leakage ventilation.
Describes the components for a single patient circuit with a patient valve.
Describes components for a double patient circuit with patient valve.
Lists and illustrates available accessories for the therapy device.
Details markings and connections on the front, right-hand side, and rear of the device.
Explains markings on the device ID plate located at the rear.
Details the device's control panel layout, buttons, and direct-access function keys.
Explains the information displayed on the device screen during operation.
Explains various symbols used in the device's status and alarm displays.
Details the specific intended uses for VENTIlogic LS and VENTIlogic plus devices.
Explains the fundamental functional aspects of the therapy device.
Lists and explains the various therapy modes available on the device.
Details the device's uninterrupted power supply via internal battery.
Specific safety warnings related to life-support ventilation and accessories.
Crucial warnings and precautions for the safe operation of the device.
Safety warnings and precautions specific to mobile operation of the device.
Safety warnings and precautions when using oxygen supply with the device.
Step-by-step guide to setting up and connecting the therapy device.
Info on interfaces and connecting for valve ventilation.
Details connecting single and double patient circuits to the device.
Instructions for connecting the device for leakage ventilation.
Guidance on connecting circuits, humidifiers, and filters to the device.
Information and warnings regarding therapy with an oxygen supply.
How to measure oxygen concentration using the sensor with valve ventilation.
How to measure oxygen saturation and pulse using the SpO2 module.
Details the device's control panel layout, buttons, and direct-access function keys.
Guide on how to navigate menus and set values using the device's dial.
Steps for starting up and preparing the therapy device for use.
Explains the information displayed on the device screen during operation.
Information on managing the internal and replaceable batteries.
Overview of the battery status within the device's patient menu.
How to activate or deactivate the auto switch-on feature for leakage ventilation.
How to view alarms and adjust display brightness.
Information on the Lung Insufflation Assist Maneuver (LIAM) function.
How to view summaries, humidifier recommendations, and LIAM details.
Steps for selecting and configuring therapy programs.
Procedures for what to do after using the therapy device.
How to check and transfer therapy data from the memory card.
Guidelines for traveling with the therapy device, particularly by air.
Details device bags and steps to prepare for mobile operation.
Specifies regular intervals for checking filters and performing hygiene tasks.
Detailed steps for cleaning the patient circuit used with leakage ventilation.
How to use the device to dry the patient circuit if it becomes wet.
Steps for cleaning the coarse dust filter and changing the fine filter.
Instructions for cleaning the fan filter and guidance on disinfection.
Disinfection recommendations for patient circuits used with leakage ventilation.
Procedures for hygiene treatment when changing patients.
Specifies the recommended intervals for performing function checks.
Outlines the general method for conducting device function checks.
Steps to check flow and pressure sensors for leakage ventilation.
Check procedure for sensors with specific leakage ventilation adapter.
Check procedure for sensors with valve ventilation.
How to check the device's alarm system functionality.
Instructions for performing a function check on the oxygen supply.
Procedure and importance of calibrating the oxygen sensor with valve ventilation.
Step-by-step guide to performing oxygen sensor calibration.
Information about the device's power supply and battery status.
Lists common faults, their causes, and recommended remedies.
Explains the different types and priorities of alarms generated by the device.
Details on specific physiological alarms, their causes, and remedies.
Details on specific technical alarms, their causes, and remedies.
Specifies intervals for recommended servicing and safety checks.
Recommended battery maintenance and replacement intervals.
Important measures to prolong battery life and maintain accuracy.
Instructions for changing the coarse dust filter.
Instructions for changing the fine filter and resetting the indicator.
Instructions for changing fan and bacteria filters.
Steps to change the pressure-measurement tube for leakage ventilation.
Details the legally specified intervals for safety checks and servicing.
Guidelines for the proper disposal of the device and its components.
Details the standard components included with the device.
Lists the standard scope of supply for the hospital version of VENTIlogic LS.
Lists the standard scope of supply for VENTIlogic plus configurations.
Detailed technical data for the therapy device itself.
Data on system resistances and specifications for bacteria filters.
Technical data for the oxygen sensor.
Technical data for the SpO2 module.
Illustrates the pneumatic pathways for different ventilation modes.
Pneumatic diagram for leakage ventilation.
Pneumatic diagram for a single patient circuit with patient valve.
Pneumatic diagram for a double patient circuit with patient valve.
Recommended safety distances for HF telecommunication devices.
Manufacturer declaration regarding electromagnetic interference emissions.
Guidelines for electromagnetic interference immunity for medical devices.
Immunity guidelines for life-supporting medical electrical systems.
Immunity guidelines for non-life-supporting medical electrical systems.
Manufacturer's declaration of product compliance with medical device directives.
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