31
SE-DV54-1
EN
guiDancE & manufacturEr’S
DEclaration
DeVilbiss GUiDanCe anD manUfaCTUReR’s
DeClaRaTion
� Warning
Medical Electrical Equipment needs special precautions regarding EMC and
needs to be installed and put into service according to the Electromagnetic
Compatibility [EMC] information provided in the accompanying documents.
Portable and Mobile RF Communications Equipment can affect Medical
Electrical Equipment.
The equipment or system should not be used adjacent to or stacked with
other equipment and that if adjacent or stacked use is necessary, the
equipment or system should be observed to verify normal operation in the
configuration in which it will be used.
The EMC tables and other guidelines provide information to the customer or user that
is essential in determining the suitability of the Equipment or System for the
Electromagnetic Environment of use, and in managing the Electromagnetic
Environment of use to permit the Equipment or System to perform its intended use
without disturbing other Equipment and Systems or non-medical electrical equipment.
Guidance and Manufacturer’s Declaration – Emissions All Equipment and
Systems
This device is intended for use in the electromagnetic environment specified below. The
customer or user of this device should assure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Enforcement – Guidance
RF Emissions
CISPR 11
Group 1
This device uses RF energy only for its internal
function. Therefore, its RF emissions are very
low and are not likely to cause any interference
in nearby electronic equipment.
RF Emissions
CISPR 11
Class B
Radiated and
Conducted Emissions
This device is suitable for use in all
establishments including domestic, and those
directly connected to the public low-voltage
power supply network that supplies buildings
used for domestic purposes.
Harmonics
IEC 61000-3-2
Class A
Flicker
IEC 61000-3-3
Complies
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