ResMed Stellar 100 Manuel D’Utilisation

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Notes: 
• The manufacturer reserves the right to change these specifications without notice.
• Pressure may be displayed in cm H
2
O or hPa.
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, 1.6 Ah, 23 Wh
Operating hours: 2 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 
*NONIN XPOD
Electromagnetic 
compatibility
Product complies with all applicable electromagnetic 
compatibility requirements (EMC) according to 
 
IEC60601-1-2, for residential, commercial, and light 
industry environments. For further details see “Guidance 
and manufacturer’s declaration – electromagnetic 
emissions and immunity” on page 29
.  
Air filter
Electro static fibre mesh with TPE frame structure. Bacterial 
filtration efficiency of 99.540% on area weight 100g/m².
Air tubing
Flexible plastic, 2 m or 3 m length (22 mm diameter)
SlimLine air tubing
Flexible plastic, 1.83 m length (15 mm diameter)
IEC 60601-1 
classifications
• Class II (Clause 3.14—double insulation). This 
adherence means the need for an protective earthing 
(ie, an earthed plug) is not necessary. 
• Type BF
• Continuous operation
Air travel requirements
Medical-Portable Electronic Devices (M-PED) that meet 
the Federal Aviation Administration (FAA) requirements 
of RTCA/DO-160 can be used during all phases of air 
travel without further testing or approval by the airline 
operator. ResMed confirms that the Stellar meets RTCA/
DO-160 requirements.
 
This device is not suitable for use in the presence of a flammable anesthetic mixture.