EN
5.2 Usage Restrictions and Limitations
The BioProTT
TM
Clamp-On SL is constructed and sold for the above-mentioned intended purpose only. The
BioProTT
TM
Clamp-On SL
is not intended
to be used:
•
for legal metrology.
•
for measuring gaseous media.
•
for measurements in explosive areas.
•
as medical device.
5.3 Liabilities and Responsibilities
The user is responsible to use, check and maintain the BioProTT
TM
Clamp-On SL according to this user manual.
em-tec GmbH is neither liable nor responsible for any consequences arising from the use of the
BioProTT
TM
Clamp-On SL that does not comply with the user manual or specifications in this document.
5.4 Safety Instructions
If the BioProTT
TM
Clamp-On SL is part of an industrial system, the user and operator have to observe the
following:
•
The measured values of the the BioProTT
TM
FlowMeasurement System report the volumetric flow rate via
the available interfaces of the respective evaluation device.
•
If the unit is used to control the liquid volume flow, the user must analyze the risk of the application
and, if necessary, take actions independent of the BioProTT
TM
FlowMeasurement System to minimize said
risk.
•
In case of an error, refer to
as well as to the user manual of the evaluation
device respectively.
5.5 Electrical Safety and Electromagnetic Compatibility
The BioProTT
TM
FlowMeasurement System (i.e. the BioProTT
TM
Clamp-On SL in combination with a
BioProTT
TM
evaluation device) represents a state-of-the-art technology. It was tested according to
IEC 61326-1: 2013
(Emission: Class A, Group 1) and
IEC 61010-1: 2010
.
Although the requirements of
IEC 61326-1: 2013
and
IEC 61010-1: 2010
were taken into account during the
development and manufacturing, the user may be at risk if the system and/or any part thereof is used
improperly.
Electrical Installation Requirements
Please follow the general safety information when installing the BioProTT
TM
FlowMeasurement System. Please
also observe any separate relevant safety and technical information of other electrical components used.
Electromagnetic Compatibility Requirements
The customer has to ensure that the relevant emission and immunity requirements of the device configuration
are ensured in accordance with the required standards.
Interference of ultrasonic flow measurements by electromagnetic fields could be possibly identified by
compromised measured data, which are not related to the real flow.
BioProTT™ Clamp-On SL
Page 8
Copyright em-tec GmbH
D162-704 BioProTT™ Clamp-On SL – User Manual– V4.0
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