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Flow measurement
Internally mounted flow transducer
Applied parts (as per IEC 60601-1)
Patient interface (Mask, endotracheal tube or tracheostomy tube)
Oximeter (optional accessory)
FiO
2
measurement
Range: 18% to 100%, Resolution: 1%, Accuracy: ± (2.5 vol.% +2.5% of actual oxygen
concentration)* (as per ISO 80601-2-55)
* The measured FiO
2
sampled at a minimum of 1Hz has a response time of 14s to 90% of
the final value. The long term output drift in 100% O
2
is typically <5% over 1 year
SpO
2
measurement
Range: 70% to 100%, Resolution: 1%, Accuracy: ±2% in a range of 70% to 100%
Pulse rate measurement
Range: 40 bpm to 240 bpm, Resolution: 1 bpm, Accuracy: Refer to Nonin Xpod technical
specifications at www.nonin.com.
Power supply
AC 100–240V, 50–60Hz, 2.2 A, max. 65 W
External DC power supply (isolated) 24 V, 3 A
Internal battery
Lithium-Ion battery, 14.4 V, 2.75 Ah, 40 Wh
Operating hours: 3 h with a new battery under normal conditions (see below).
Patient type: home chronic; pressure: IPAP/EPAP 15/5 cm H
2
O; mask type: Ultra Mirage; air
tubing: 2 m; leak: 0; respiratory rate: 20 bpm; battery capacity: 100%
Patient type: hospital acute; pressure: IPAP/EPAP 20/5 cm H
2
O; mask type: Ultra Mirage; air
tubing: 2 m; leak: 0; respiratory rate: 45 bpm; battery capacity: 100%
Housing construction
Flame retardant engineering thermoplastic
Environmental conditions
•
Operating temperature: 0°C to 35°C
•
Operating humidity: 10%–95% non-condensing
•
Storage and transport temperature: -20°C to 60°C (+50°C*)
•
Storage and transport humidity: 10%–95% non-condensing
•
Air pressure: 680hPa to 1,100hPa; Altitude: 3,000 m
Note:
The performance may be limited below 800 hPa.
*NONIN XPOD
Electromagnetic compatibility
The device complies with all applicable electromagnetic disturbances requirements (EMD)
according to IEC 60601-1-2:2014, for residential, commercial and light industry
environments.
It is recommended that mobile communication devices are kept at least 0.3 m away from
the device.
Information regarding the electromagnetic emissions and immunity of this ResMed device
can be found in www.resmed.com/downloads/devices.
Potential impact of electromagnetic
disturbances
The loss or degradation of the following clinical functions due to electromagnetic
disturbances could result in compromised patient safety:
•
Accuracy of ventilation control
•
Accuracy of monitoring of airway pressure and volume
•
Therapy alarms
Detection of this degradation could be observed by the following device behaviour:
•
Erratic ventilation delivery
•
Rapid fluctuations in monitored parameters
•
False activation of therapy or technical alarms
Summary of Contents for Stellar 100
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