
Dräger · Model Primus
Personal anaesthesia assistant - The Dräger Primus was designed to be nothing less than your personal anaesthesia assistant. It’s a combination of time-tested design and state-of-the-art technology created to answer the demand for a modern, comprehensive anaesthesia solution for today’s increasingly complex healthcare environment. Common operating philosophy - The Primus® uses the familiar user interface and operating philosophy common to all current Dräger medical devices. This means that in spite of its impressive level of sophistication, your staff will spend a minimum amount of time learning how to use the Primus. Enhanced workflow - Features like fully automatic self-check, open architecture, standard user interfaces and flexible monitoring options were designed to help reduce costs, save time and allow caregivers to focus on their primary task – the patient. ICU standard ventilation - An increasing percentage of critically ill patients in the operating room calls for new standards in anaesthesia platforms. With the E-Vent® plus high-speed electronic piston ventilator, the Primus® delivers just that – peak flow comparable to ICU ventilators while avoiding the need for drive gas. A full range of volume and pressure oriented modes provides the various options for every clinical situation. Additional advanced monitoring and ventilation mode packages are also available that will expand your capabilities. Comprehensive monitoring - The Dräger Primus?® lets you monitor pulmonary function and ventilation parameters on a large, user-configurable 12,1“TFT colour display. Its open architecture design provides the option to add additional displays, permitting you to expand your monitoring capability to include haemodynamic and other data.
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.
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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