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Notes:
• The manufacturer reserves the right to chan
ge 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
Sup
ply (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 therm
oplastic
Environmental
con
ditions
• 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-
cond
ensing
• Air pressure: 680hPa to 1,100hPa; Altitude: 3,000 m
*NONIN XPOD
Electromagnetic
compatib
ility
Product complies with all applicable electromagnetic
compatibility requirements (EMC) according to
IEC60601-1-2, for residential, comm
ercial, and light
industry environments. For further details see “Guidance
and manufacturer’s declaration – ele
ctromagnetic
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
clas
sifications
• 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 F
ederal 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 p
resence of a flammable anesthetic mixture.