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RIDA qLine® Orbital Shaker | User Manual
8 Troubleshooting/information on reporting to
authorities
For users in the European Union: Report all serious adverse events associated with the
product to R-Biopharm AG and the appropriate national authorities.
9 Conformity to IEC 61326-2-6 and RoHS3
The CE mark on the RIDA qLine® Orbital Shaker confirms that the RIDA qLine® Orbital
Shaker is compliant with Regulation (EU) 2017/746 (
In Vitro
Diagnostic Medical Devices).
In addition, the RIDA qLine® Orbital Shaker fulfills the protection requirements of EMC
pursuant to IEC 61326-2-6. The RIDA qLine® Orbital Shaker is complaint with the current
RoHS Directive.
