Air travel requirements
This device is not suitable for use in the presence of a flammable anesthetic mixture.
Notes:
•
The manufacturer reserves the right to change these specifications without notice.
•
Pressure may be displayed in cm H
Symbols
Follow instructions for use;
Alarm); IP31 Device is protected against solid foreign objects of 2.5 mm diameter and greater and
vertically falling water drops;
connection on the device);
oxygen supply; max 30 l/min (max 30 L/min);
directive 93/42/EEC, class II b;
care;
Maximum humidity;
Batch code;
Use by date;
China environmental hazardous substances.
Environmental information
This device must be disposed of in accordance with the laws and regulations of the country in which
disposal occurs.
The crossed-out wheeled bin symbol
disposed of together with general household waste, but instead requires separate disposal. This
requirement for separate disposal is based on the European Directive 2012/19/EU for electrical and
electronic equipment, and the European Directive 2006/66/EC for batteries. You can hand in the product at
a municipal collection point, for example. This reduces the impact on natural resources and prevents
contamination of the environment through the release of hazardous substances.
Batteries containing more than 0.0005 percent of mercury by mass, more than 0.002 percent of cadmium
by mass or more than 0.004 percent of lead by mass are marked below the crossed- bin symbol with the
chemical symbols (Hg, Cd, Pb) of the metals for which the limit is exceeded.
For further information regarding product disposal, please contact your local ResMed office or your
specialist distributor, or visit our website at www.resmed.com.
Dispose of used air filters and air tubings according to the directives in your country.
32
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.
O or hPa.
2
Class II equipment;
Caution;
Standby or preparatory state for a part of equipment;
Temperature limitation for storage and transport;
Keep dry;
Do not re-use;
Do not use if package is damaged;
Keep away from sunlight;
indicates that the product bearing this symbol may not be
Type BF applied part;
General warning sign (see H4i connector plug and AC
Data port;
CE labeling in accordance with EC
Manufacturer;
Latex-free;
MR unsafe (do not use in the vicinity of an MRI device).
Bell (Remote
Connection for
Handle with
Upside;
Serial number;
Catalogue number;
Device weight;
Contains no