
CareFusion · Model Pulmonetics LTV 1100
High performance ventilation in a small lightweight package (10” x 12” x 3”, 13.4 lbs). Turbine technology allows the LTV Series ventilator to operate without an external compressed gas source. CPAP5, SIMV6, Control, Assist / Control and Apnea Backup ventilation modes. NPPV7 mode ventilation, providing an alarm package suitable for mask ventilation of patients that do not require life support ventilation. Volume Control, Pressure Control (optional) and Pressure Support ventilation. Variable alarm settings including High Peak Pressure, Low Peak Pressure, Low Minute Volume, Apnea, High Breath Rate, and High PEEP. Oxygen Blending from a High-Pressure Oxygen source, Low-Pressure Oxygen Bleed-in, O2 Flush, and O2 Cylinder Duration Monitoring on the LTV 1000, and Low-pressure Oxygen Bleed-in on the LTV 950 and 900. Lockable front panel controls. Monitors for Breath Rate (f), I: E Ratio, MAP, Minute Ventilation (VE), PEEP, PIP and Tidal Volume (Vte). Real-time patient circuit pressure display with Peak Inspiratory Pressure indicator. Variable termination conditions for Pressure Support breaths, including maximum inspiratory time termination and percentage of peak flow. Selectable Percentage of Peak Flow termination for Pressure Control breaths. Leak Compensation to improve triggering when a circuit leak is present. Single or dual tone output capabilities. Operation from a variety of power sources including AC power, internal battery and external DC power sources.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Self-test fault, circuit-leak or compliance-check failure, will not be released for use.
Root cause: Patient-circuit / expiratory-valve leak, a flow-sensor fault, an O2-cell fault, or an internal pneumatic fault.
Symptoms: Delivered tidal volume or flow does not match the setting, or fails the annual verification.
Root cause: Flow-sensor drift / contamination, an inspiratory / expiratory valve fault, or a blender / proportioning-valve fault.
Symptoms: Low-supply alarm, FiO2 not matching the setting, O2-cell reads wrong.
Root cause: Wall / cylinder supply issue, an inlet filter / regulator fault, the blender, or an aged O2 cell.
Symptoms: PEEP drifts, auto-PEEP, high-pressure alarms, poor exhalation.
Root cause: Worn or wet expiratory valve / diaphragm, or a blocked exhalation path.
Symptoms: Short internal-battery run time, will not charge, transfers to battery unexpectedly.
Root cause: Aged internal battery or a power-supply fault.
Symptoms: Noisy operation, cannot meet flow demand, turbine / compressor alarm.
Root cause: Worn turbine / compressor.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Flow sensor(s) | Frequent wear item | $$ | Fairly easy |
| Expiratory valve / diaphragm | Frequent wear item | $$ | Fairly easy |
| O2 cell / sensor | Frequent wear item | $$ | Easy |
| Internal battery | Periodic replacement | $$ | Fairly easy |
| Inlet filters / water traps | Frequent wear item | $ | Easy |
| Turbine / compressor (turbine units) | Major service part | $$$$ | Difficult |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
No documents available for this device yet.
From BioLab, for work done with this kind of equipment.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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