26
Air filter
Electrostatic fibre mesh with TPE frame structure. Bacterial filtration efficiency of >99.9%
for ~2.7 micron particle size.
Air tubing
Standard air tubing: Flexible plastics, 2 m or 3 m length (22 mm diameter)
SlimLine air tubing: Flexible plastics, 1.83 m length (15 mm diameter)
For more information on air tubing resistance to flow, compliance, tubing length, and inner
diameter, refer to the Air tubing compliance guide in ResMed.com.
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.
Notes:
•
The manufacturer reserves the right to change these specifications without notice.
•
Pressure may be displayed in cm H
2
O or hPa.
Symbols
Follow instructions for use;
Class II equipment;
Type BF applied part;
Bell (Remote
Alarm);
IP31
Device is protected against solid foreign objects of 2.5 mm diameter and greater and
vertically falling water drops;
Caution;
General warning sign (see H4i connector plug and AC
connection on the device);
Standby or preparatory state for a part of equipment;
Connection for
oxygen supply;
(max 30 L/min);
Data port;
CE labeling in accordance
with EC directive 93/42/EEC, class II b;
Temperature limitation for storage and transport; Handle
with care;
Maximum humidity;
Keep dry;
Manufacturer;
Upside;
Serial number;
Batch code;
Do not re-use;
Do not use if package is damaged;
Catalogue number;
Use by date;
Keep away from sunlight;
Latex-free;
Device weight;
Contains no
China environmental hazardous substances.
MR unsafe (do not use in the vicinity of an MRI device).
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
indicates that the product bearing this symbol may not be
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.
Summary of Contents for Stellar 100
Page 212: ...2 1 I 2 1 J 1 2 3 4 5 K ...
