
Datex Ohmeda · Model Aespire 7900
Unparalleled ventilation Advanced ventilation modes include PSVPro System is lightweight and compact for easy maneuverability Large work surface offers more room for supplies and chart LED light strip provides bi-level work surface illumination Bellows provide quick visual confirmation of the integrity of breathing system High-quality pneumatic flow mixing Auxiliary common gas outlet facilitates low-pressure leak test PSV Pro Assists in overcoming the resistance within the breathing circuit and patient circuit, helping decrease the patient's work of breathing Helps counter the reduction in the patient’s functional residual capacity (FRC) and the decrease in muscle contraction due to the anesthetics May be used with LMAs due to its lower airway pressures With automatic apnea backup mode, uses an SIMV-PC + PSV mode to maintain a minimum minute ventilation in the event the patient stops spontaneously breathing. With adjustable inspiration termination, allows fine-tuning to the patient’s breathing pattern. Supports virtually all spontaneous breaths Uses a decelerating flow pattern (optimizes inspiratory flow) Sustains or enhances the patient’s tidal volume and etCO2 maintenance.
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: Low-pressure or circle-system leak test fails, machine not ready for use.
Root cause: Breathing-circuit / absorber leak, a worn APL valve or bag arm, a CO2-absorber canister seal, or a vaporiser back-bar leak.
Symptoms: Set tidal volume not delivered, bellows will not fill or hangs up, piston fault, PEEP not held.
Root cause: Bellows leak, a drive-gas valve fault, a flow-sensor fault, or a piston-seal fault.
Symptoms: O2 flow not matching the setting, flowmeter float sticking, hypoxic-guard / ratio fault, no O2 flush.
Root cause: Worn flowmeter (rotameter), a hypoxic-guard link fault, or a flush-valve fault.
Symptoms: Agent output does not match the dial, back-bar leak, dial stiff.
Root cause: Vaporiser seating / O-ring, or an internal vaporiser fault (calibrate at an authorised centre).
Symptoms: O2-failure whistle / alarm, anti-hypoxia device cuts N2O, pipeline-pressure fault.
Root cause: Loss of pipeline / cylinder pressure, or a pressure-sensor fault.
Symptoms: Waste-gas scavenging alarm or not evacuating, theatre pollution.
Root cause: Scavenging flow / connection or a receiver-valve fault.
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 |
|---|---|---|---|
| APL valve / breathing-system gaskets & seals | Periodic replacement | $$ | Fairly easy |
| CO2 absorbent / canister seals | Consumable | $ | Easy |
| Ventilator bellows / piston seal | Major service part | $$$ | Difficult |
| Flow sensor(s) | Frequent wear item | $$ | Fairly easy |
| O2 flowmeter (rotameter) | Major service part | $$ | Moderate |
| Vaporiser O-ring / back-bar seal | Periodic replacement | $ | Fairly easy |
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.
Extracted directly from this unit's own service manual.
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.
Synced live from the FDA openFDA API.
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
Elevated inspired CO2 levels related to the use of the Datex-Ohmeda GE Healthcare Disposable Multi Absorber Canister with the EZchange Module.
Two conditions may occur with the S/5 Aespire Anesthesia System. The internal auxiliary flowmeter tubing may become disconnected if the auxiliary oxygen supply tubing is occluded and the patient may not receive desired supplemental oxygen which could lead to serious injury if undetected. Also the O2 switch may leak or fail.
Increased circuit pressure as a result of a misassembled Aestiva/5 Active Gas Scavenging System.
Multi Absorbers for anesthesia delivery equipment may have missing or damaged filters, exposing the patient to dust from soda lime in the absorbers.
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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