R-Biopharm RIDA QUICK SCAN II, Руководство пользователя

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Only replacement parts and accessory components that are authorized by the
manufacturer may be used.
Always check the power supply for damage before using the RIDA®QUICK SCAN II. The
mains unit must be replaced immediately in case of defects such as damaged insulation,
crushing or obvious kinks.
If you are unsure, please contact your local distributor or
R-Biopharm, Darmstadt, directly.
Warning: The proper function of the RIDA®QUICK SCAN II and the safety of the
device cannot be guaranteed in the event of nonobservance of the safety
information.
R-Biopharm shall not assume any liability for damage to the device or accessories
or other property damage or personal injury resulting from failure to observe the
safety information. In such cases, all
warranty claims against R-Biopharm are null
and void.
EC Declaration of conformity/CE mark
The CE Mark of the RIDA®QUICK SCAN II confirms that the RIDA®QUICK SCAN II is in
compliance with Regulation (EU) 2017/746 (“
In Vitro Diagnostic Medical Devices”).
In addition, the RIDA®QUICK SCAN II is compliant with the current RoHS Directive and
conforms to standards DIN EN 55011 and DIN EN 61326-2-6 on radio-frequency
disturbance characteristics of industrial, scientific, and medical equipment and to the
directive. The RIDA®QUICK SCAN II was developed and tested in accordance with
CISPR 11 Class A. It may cause radio interference in a domestic environment. In this case
it may be necessary to take measures to eliminate the interference.