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 CAP Bac

Intended use:For in vitro diagnostic use. RIDA®GENE CAP Bac is a multiplex real-time PCR for the direct qualitative detection and differentiation of Chlamydophila pneumoniae (Chlamydia [...]

RIDA®GENE Enterovirus

Intended use:For in vitro diagnostic use. RIDA®GENE Enterovirus is a multiplex real-time RT-PCR for the direct qualitative detection of Enterovirus from human stool samples and cerebrospinal [...]

RIDA®GENE Adenovirus

Intended use:For in vitro diagnostic use. RIDA®GENE Adenovirus is a multiplex real-time PCR for the direct, qualitative detection of Adenovirus in human stool samples, throat rinsing fluid, [...]

RIDA®GENE Sapovirus

Intended use:For in vitro diagnostic use. RIDA®GENE Sapovirus is a multiplex real-time RT-PCR for the direct, qualitative detection of sapovirus from human stool samples. RIDA®GENE Sapovirus [...]

RIDA®GENE Legionella

Intended use:For in vitro diagnostic use. RIDA®GENE Legionella is a multiplex real-time PCR for the direct, qualitative detection and differentiation of Legionella pneumophila and Legionella spp. [...]

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 [...]

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