Pari eFlow rapid Instrucciones De Uso página 325

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
environment.
Electromagnetic emissions
Emission test
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations /
flicker emissions
IEC 61000-3-3
®
eFlow rapid - 03/12
Compliance Electromagnetic environment – Guidance
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
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.
Not applicable
Passed
®
rapid should assure that it is used in such
®
rapid is suitable for use in all
Table 1 of DIN EN 60601-1-2:2007 (IEC 60601-1-2:2007)
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