GUIDANCE AND MANUFACTURER’S DECLARATION - ELECTROMAGNETIC EMISSIONS AND IMMUNITY
Guidance and manufacturer’s declaration – electromagnetic emissions
The ResMed S7 Lightweight is intended for use in the electromagnetic environment specified below. The customer or the user of the ResMed S7 Lightweight should assure that it is used in such an environment.
Emissions test | Compliance | Electromagnetic environment - | |
guidance | |||
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RF emissions CISPR11 | Group 1 | The ResMed S7 Lightweight uses RF | |
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| energy only for its internal function. | |
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| Therefore, its RF emissions are very low | |
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| and are not likely to cause any | |
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| interference in nearby electronic | |
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| equipment. | |
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RF emissions CISPR 11 | Class B | The ResMed S7 Lightweight is suitable | |
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| for use in all establishments, including | |
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Harmonic Emissions | Class A | domestic establishments and those | |
IEC |
| directly connected to the public low- | |
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| voltage network that supplies buildings | |
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Voltage Fluctuations/Flicker | Complies | used for domestic purposes. | |
Emissions IEC |
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Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and put into service according to EMC information provided in this document.
Warnings: The ResMed S7 Lightweight should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the ResMed S7 Lightweight should be observed to verify normal operation in the configuration in which it will be used.
The use of accessories (eg Humidifiers) other than those specified in this manual is not recommended. They may result in increased emissions or decreased immunity of the ResMed S7 Lightweight.
ENGLISH
SYSTEM SPECIFICATIONS | 25 |
