
Dräger · Model Oxylog 2000 Plus
Built for demanding situations - In the field and in emergency situations, reliability, rugged design and simple operation are vital factors for success. The Dräger Oxylog® 2000 plus was designed to provide the caregiver with powerful and flexible ventilation capabilities under the most demanding conditions. Intuitive user interface - The large display gives you clear and highly visible information on clinical values, airway pressure and parameter settings, allowing rapid evaluation of the patients condition during hectic situations. Intuitive controls enable operation within seconds after starting the device. Standardised equipment - The Oxylog® 2000 plus uses the same standardised reusable and disposable hoses as the Oxylog® 3000, letting you simplify your inventory and workflow. Ventilation essentials at your fingertips - The Oxylog® 2000 plus gives you not only a selection of volume-controlled modes but also offers support modes for both invasive and non-invasive ventilation. Pressure Support and Non-Invasive Ventilation are available, enabling support for patients with insufficient breathing and to help prevent intubation at the earliest stage possible. Rugged, compact and highly portable - Easy to carry and simple to mount, the Oxylog® 2000 plus was specifically designed to be taken nearly anywhere. Built from extremely durable, high-impact materials, the unit can stand up to even the most challenging environments. The internal battery provides up to 4 hours of autonomous transport capability.
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.
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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