Newport Medical e360
Newport Medical · Model e360
Newport NMI e360 Ventilator.
Key tips
- ·Never disable a low-pressure/circuit-disconnect alarm while troubleshooting - silence it, don't disable it.
- ·Verify the O2 supply source and pressure before assuming an internal fault.
- ·Circuit type must match the patient population (adult/pediatric/neonatal) - a mismatched circuit invalidates delivered volumes.
Typical Failure Modes
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.
Fails the pre-use self-test / circuit check
HighSymptoms: 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.
Flow / volume delivery inaccurate
HighSymptoms: 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.
O2 / air supply or blender fault
MediumSymptoms: 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.
PEEP not held / high circuit pressure
MediumSymptoms: PEEP drifts, auto-PEEP, high-pressure alarms, poor exhalation.
Root cause: Worn or wet expiratory valve / diaphragm, or a blocked exhalation path.
Battery / power fault
MediumSymptoms: Short internal-battery run time, will not charge, transfers to battery unexpectedly.
Root cause: Aged internal battery or a power-supply fault.
Turbine / compressor fault (turbine units)
MediumSymptoms: Noisy operation, cannot meet flow demand, turbine / compressor alarm.
Root cause: Worn turbine / compressor.
Serviceable Parts & Consumables
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.
Flow sensor(s)
Class Frequent wear itemRel. cost $$R&R Fairly easy
Expiratory valve / diaphragm
Class Frequent wear itemRel. cost $$R&R Fairly easy
O2 cell / sensor
Class Frequent wear itemRel. cost $$R&R Easy
Internal battery
Class Periodic replacementRel. cost $$R&R Fairly easy
Inlet filters / water traps
Class Frequent wear itemRel. cost $R&R Easy
Turbine / compressor (turbine units)
Class Major service partRel. cost $$$$R&R Difficult
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Flow sensor(s) | Frequent wear item | $$ | 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.
PM Checklist
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.
- ·Daily pre-use check: self-test, circuit integrity, alarm function
- ·Scheduled circuit and inspiratory filter replacement per manufacturer interval
- ·Flow and pressure sensor calibration verification
- ·Battery load test and runtime check
- ·Annual full PM and electrical safety test
Error Codes
Extracted directly from this unit's own service manual.
No audible alarmNo audible alarm. Defective alarm speaker, Sound processor board or SBC.
Replace alarm speaker or sound processor board or SBC.
Control task continuity failureControl Tasks Failed High. Software tasks of the control processor have operated out of sequence.
Dual RAM failureDual RAM Failed High. Random access memory that is shared between the control and monitor processors is damaged.
Monitor communications failureControl uP Failed High. The control processor does not respond to a request from the Monitor processor. The control processor is not running.
Monitor CPU failureMonitor CPU Failed High. The monitor processor on the main PCB is bad.
Monitor exception failureMonitor exception failure C Internal System High. The monitor processor has detected an abnormal operation such as illegal instruction or division by zero that was generated by the monitor software.
Monitor RAM failureMonitor RAM Failed High. Random access memory that is used by the monitor processor on the main PCB is damaged.
Monitor ROM failureMonitor ROM Failed High. Read only memory that stores the code of the monitor processor has an incorrect checksum.
Monitor task continuity failureMon Task Failed High. Software tasks of the monitor processor have operated out of sequence.
Power FailurePower Failure High. DC power out of tolerance. Check +12 VDC, –12 VDC and +5 VDC. (The e360 may have been powered by internal battery until it was depleted and a Device Alert resulted.)
Check +12 VDC, –12 VDC and +5 VDC.
Troubleshooting Approach
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.
Symptom: Fails the pre-use self-test / circuit check
- Run the self-test with the exact circuit, filter and humidifier that will be used.
- Leak-test the circuit and the expiratory valve; fit fresh flow sensors and an O2 cell if due.
- Repeat the self-test and note which check fails.
- Calibrate the flow sensors and O2 cell per the manual.
- Remove from service and refer an internal pneumatic fault to the OEM / biomed.
Symptom: Delivered tidal volume / flow or FiO2 inaccurate
- Verify tidal volume and flow with a calibrated gas-flow analyser and FiO2 at the wye with an O2 analyser.
- Calibrate the flow sensors and the O2 cell.
- Inspect the inspiratory and expiratory valves / diaphragms.
- Check the air and O2 supply pressures and the inlet filters / water traps.
- Refer the blender / proportioning valve if the mix is still wrong.
Symptom: PEEP not held / high circuit-pressure or auto-PEEP
- Inspect the expiratory valve / diaphragm for wear or moisture and replace it.
- Check the exhalation path and the expiratory flow sensor.
- Confirm the circuit and water trap are not obstructed.
- Run the valve / compliance calibration.
- Re-verify PEEP against the analyser.
Symptom: Low-supply / O2 alarm or turbine / compressor fault
- Confirm wall / cylinder supply pressure and the inlet hose and filter.
- Check the internal blender / regulator.
- For a turbine unit, listen for turbine noise and check it can meet flow demand.
- Replace the O2 cell if the FiO2 reading is the issue.
- Refer the turbine / compressor for replacement if it cannot meet demand.
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- ICU / CCU
- Emergency Department
- Operating Room (anesthesia-adjacent)
- NICU
- Respiratory Therapy department
- Patient transport
Documents & Manuals
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
The recall was initiated due to a recent increase in complaints related to the early failure of a low pressure transducer which is on Printed Circuit Board (PCB) 2104A in the Newport e360 ventilator. Ventilators manufactured between September and December 2009 are affected by this field correction. All affected ventilators require the replacement of the PCB2104A board to avoid early failure of t
- RECALL
Cregarding e360 ventilators that were shipped with a different software version from what the customers ordered.
- RECALL
In December 2008, Newport initiated a field correction to upgrade e360 ventilators with software versions 3.0 or higher to software version 3.3. As a result of this upgrade, some customers experienced unexpected device alert alarms. Newport's investigation into these complaints confirmed that the 3.3 software responds too quickly to certain situations, giving a false device alert. Newport condu
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