ResMed S8 Escape II CPAP
ResMed · Model S8 Escape II CPAP
• Whisper-quiet motor - Setting a new industry standard in quiet therapy and comfort, ResMed’s new sophisticated motor design delivers superior performance at a lower effort while cutting device noise significantly. By reducing noise, Easy-Breathe technology enables patients and their bed partners to sleep peacefully through the night. • Easy-Breathe technology - Easy-Breathe technology combines new software, a quieter motor and improved EPR with Easy-Breathe for maximum comfort and a quiet night’s sleep. • Pressure relief for more natural breathing - Featuring ResMed’s improved EPR with Easy-Breathe technology, the S8 Escape II offers pressure relief delivered in a smooth waveform that mimics patient breathing. With a choice of three different EPR comfort levels, the S8 Escape II with Easy-Breathe technology allows customized comfort for breathing that feels natural. • Why prescribe EPR with Easy-Breathe? - Not all CPAP devices with pressure relief are the same. ResMed’s EPR with Easy-Breathe technology is supported by clinical studies, proving it as clinically effective as traditional fixed CPAP, but significantly more comfortable. EPR is preferred over traditional CPAP by 79% of patients.
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
Failure patterns typical of this equipment class - general BMET reference, not verified against this exact unit's own service history unless flagged. Severity is a category-level estimate.
Flow / pressure sensor drift
MediumSymptoms: Inaccurate delivered volume, false volume/pressure alarms.
Root cause: Sensor contamination or aging of differential-pressure transducer.
Compressor / turbine failure
HighSymptoms: Unable to reach set pressure, low-flow alarm, loud noise.
Root cause: Worn bearings or failed blower motor.
Power supply / battery failure
HighSymptoms: Unexpected shutdown, persistent low-battery alarm.
Root cause: Aged internal battery or failed PSU.
Patient circuit leak
LowSymptoms: Leak alarm, low circuit pressure, volume loss.
Root cause: Disconnected or punctured patient circuit / humidifier.
Serviceable Parts & Consumables
The parts a BMET typically services on this class of equipment. Service class and relative cost are general engineering estimates for the category, not figures from this unit's documentation. Part numbers appear only when pulled from this unit's own service manual. Always confirm intervals and pricing against the manufacturer.
Rechargeable battery pack
Class Periodic replacementRel. cost $$R&R Fairly easy
O2 sensor (galvanic/paramagnetic)
Class Frequent wear itemRel. cost $$R&R Fairly easy
Exhalation valve assembly
Most-replaced wearable part; stock spares.
Class Frequent wear itemRel. cost $$R&R Fairly easy
Flow / differential pressure sensor
Class Periodic replacementRel. cost $$$R&R Moderate
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Rechargeable battery pack | Periodic replacement | $$ | Fairly easy |
| O2 sensor (galvanic/paramagnetic) | Frequent wear item | $$ | Fairly easy |
| Exhalation valve assembly Most-replaced wearable part; stock spares. | Frequent wear item | $$ | Fairly easy |
| Flow / differential pressure sensor | Periodic replacement | $$$ | Moderate |
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
Troubleshooting Approach
A structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Symptom: Exhalation valve leak / failure
- Confirm the presentation - typically low exhaled tidal volume, high leak alarm, inability to maintain PEEP - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: diaphragm/valve degraded by secretions and cleaning cycles.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the exhalation valve assembly per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Symptom: Flow / pressure sensor drift
- Confirm the presentation - typically inaccurate delivered volume, false volume/pressure alarms - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: sensor contamination or aging of differential-pressure transducer.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the flow / differential pressure sensor per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
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
No documents available for this device yet.
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
S8 devices manufactured between July 2004 and May 15, 2006 are susceptible to fatigue in the connection of the AC appliance inlet connector and the power supply (power cord) leading to possible failure (short circuit, electrical failure, sparks, smoke).
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