
GE HealthCare · Model Aestiva 7900
The Aestiva* breathing circuit is integrated, which helps protect the components from damage and disconnection. Smart sensors and switches link communication between the breathing circuit and the. SmartVent* ventilator. Get close to your patient with monitors that are easily viewed and controls that are conveniently located, whether you are sitting or standing. Aestiva’s open architecture means it can fit easily with your existing equipment, monitors and accessories included. Enhanced Workflow Aestiva offers a cost-effective approach to anesthesia therapy and workflow through. Low planned maintenance requirements and durable components to improve uptime. An effective system for the practice of low-flow anesthesia, helping to minimize agent consumption to help save on anesthetic agent costs.
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.
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.
Synced live from the FDA openFDA API.
The alarm timer is reset after each exposure and therefore never reaches the five minute alarm state unless one exposure exceeds 5 minutes in duration.
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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