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®UNITY SARS-CoV-2 DT

Intended use:For in vitro diagnostic use. The RIDA®UNITY SARS-CoV-2 DT test, performed automatically or manually, is a multiplex real-time RT-PCR for the direct qualitative detection of: – [...]

RIDA®GENE Flu & SARS-CoV-2

Intended use:For in vitro diagnostic use. The RIDA®GENE Flu & SARS-CoV-2 test, performed on the LightCycler® 480II real-time PCR instrument, is a multiplex real-time RT-PCR for the direct [...]

RIDA®GENE SARS-CoV-2

Intended use:For in vitro diagnostic use. The RIDA®GENE SARS-CoV-2 test, which will be performed on the Roche LightCycler® 480II, is a multiplex real-time RT-PCR for the direct qualitative [...]

RIDA® Anreicherungsbouillon

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Intended use:For in vitro diagnostic use. The RIDA® Anreicherungsbouillon is used for the enrichment of bacteria that produce verotoxin 1 and verotoxin 2 (synonyms: Shiga toxin 1 and Shiga toxin [...]

RIDA qLine® Incubation Set

Intended use: One incubation set consists of 1 strip holder for fixation of up to 10 RIDA qLine® Allergy strips and one cover lid for dark incubation on the RIDA qLine® Allergy Orbital Shaker. [...]

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