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14 Corrective action/Notification to authorities
For users in the European Union: Serious incidents occurring in the context of the product
must be reported to R-Biopharm AG and the responsible national authority.
15 Technical Support
For all technical support and assistance, contact:
R-Biopharm AG
An der neuen Bergstraße 17
64297 Darmstadt
Germany
+49 (0) 61 51 - 8102-0
www.r-biopharm.com
Only by R-Biopharm AG or associated trained service personnel may authorized repairs
and servicing be carried out.
For further details of instrument or to arrange for training to be given on the instrument,
contact R-Biopharm AG at the above address.
16 Conformity IEC 61326-2-6 and RoHS3
The CE marking of the RIDA qLine® autoBlot confirms that the RIDA qLine® autoBlot
is compliant with Regulation (EU) 2017/746 (“In Vitro Diagnostic Medical Devices”).
In addition, the RIDA qLine® autoBlot is compliant with the current RoHS Directive
and meets the standard IEC 61326-2-6.
