
GE HealthCare · Model Nellcor Oximax DAS
Assembly module This Module comes with Nellcor Oximax SPO2, NIBP, ECG, NIBP, Temperature and IBP Invasive Blood Pressure. DAS Module goes in GE Dash 3000, Dash 4000 and GE Dash 5000 Monitors.
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: Agent, CO2, N2O, O2 or SpO2 values off vs a reference, calibration prompts.
Root cause: Sensor aging, a missed calibration, or the wrong calibration gas.
Symptoms: Host monitor does not display the module or Tram / pod.
Root cause: Docking / rack connector or cable fault.
Symptoms: Occlusion or water-trap alarm, no or low sample flow, flat waveforms.
Root cause: Full or expired water trap, or a blocked / kinked sample line.
Symptoms: Intermittent signal with cable movement.
Root cause: Worn patient cable.
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 |
|---|---|---|---|
| Patient cable set | Frequent wear item | $$ | Easy |
| Water trap / sample line | Consumable | $ | Easy |
| O2 sensor / gas bench service | Frequent wear item | $$ | Fairly easy |
| Module / Tram / pod docking connector | Major service part | $$ | Moderate |
| Internal sample pump | Periodic replacement | $$$ | Difficult |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
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.
No documents available for this device yet.
Synced live from the FDA openFDA API.
Medical device software may be defective and may cause user-set alarm limits to result in false positive or false negative Oxygen saturation and pulse rate alarm notifications to the caregiver.
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