Dear customers,

we have started to provide the documents for our products in an electronic format. These are the Instructions for Use (IFU), the Safety Data Sheets (SDS) and the Certificate of Analysis (CoA). For batches placed on the market after 01 January 2023, you can find our documents on the eIFU portal https://eifu.r-biopharm.com.

RIDA®GENE RSV & hMPV

Intended use:For in vitro diagnostic use. The RIDA®GENE RSV & hMPV test, performed on Roche LightCycler® 480 II, is a multiplex real-time RT-PCR for the direct qualitative detection and [...]

RIDA®GENE Faecalibacterium prausnitzii

Intended use:For in vitro diagnostic use. RIDA®GENE Faecalibacterium prausnitzii is a multiplex real-time PCR for the direct qualitative and quantitative detection of Faecalibacterium prausnitzii [...]

RIDA® CCD-Inhibitor

Intended use:The RIDA® CCD-Inhibitor is an accessory for use in in vitro diagnostics for the inhibition of anti-CCD IgE in human serum and plasma. General information:CCDs (cross-reactive [...]

RIDA®QUICK IFX Monitoring Control Set

Intended use:For in vitro diagnostic use. The RIDA®QUICK IFX Monitoring Control Set is intended for the use with the corresponding, batch specific kit RIDA®QUICK IFX Monitoring (GN3041). General [...]

RIDA®QUICK SCAN II

Intended use:For in vitro diagnostic use. The RIDA®QUICK SCAN II is a lateral flow reader for automatic reading of quantitative lateral flow tests. Use the RIDA®QUICK SCAN II only in combination [...]

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