eFlow
®
rapid
- 03/12
321
de
Electromagnetic compatibility -
Guidance and manufacturer's declaration
DIN EN 60601-1-2:2007 (IEC 60601-1-2:2007)
Medical electrical devices are subject to special precautionary measures in particular
regarding the EMV with the installation and the operation.
Portable and mobile HF-communication devices e.g. mobile phone can affect medical
electrical devices.
A use of other accessories and lines than the indicated, can lead to an increased sen-
ding or a reduced noise immunity of the equipment. The equipment has to be operated
exclusively with original accessories.
The device should not be used adjacent to or stacked with other equipment. If adjacent
or stacked use is necessary, the device should be observed to verify normal operation
in the configuration in which it will be used.
Electromagnetic environment
The eFlow
®
rapid
is intended for use in the electromagnetic environment specified
below. The customer or the user of the eFlow
®
rapid
should assure that it is used in such
environment.
Electromagnetic emissions
Emission test
Compliance
Electromagnetic environment – Guidance
RF emissions
CISPR 11
Group 1
The device uses RF energy only for its inter-
nal function. Therefore, its RF-emission is
very low and not likely to cause any interfer-
ence nearby electronic equipment.
Class B
The eFlow
®
rapid
is suitable for use in all
establishments, including domestic establish-
ments and those directly connected to the
public low-voltage power supply network that
supplies buildings used for domestic pur-
poses.
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage fluctuations /
flicker emissions
IEC 61000-3-3
Passed
Table 1 of DIN EN 60601-1-2:2007 (IEC 60601-1-2:2007)
Summary of Contents for eflowrapid 178G1005
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