RIDA®GENE Bacterial Stool Panel I
Intended use:For in vitro diagnostic use. RIDA®GENE Bacterial Stool Panel I is a multiplex real-time PCR for the direct, qualitative detection and differentiation of STEC, Salmonella spp., [...]
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.
Intended use:For in vitro diagnostic use. RIDA®GENE Bacterial Stool Panel I is a multiplex real-time PCR for the direct, qualitative detection and differentiation of STEC, Salmonella spp., [...]
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 [...]
Intended use:For in vitro diagnostic use. RIDA®GENE Akkermansia muciniphila is a multiplex real-time PCR for the direct qualitative and quantitative detection of Akkermansia muciniphila DNA from [...]
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 [...]
Intended use:RIDASCREEN® Anti-IFX Antibodies is an enzyme linked immunoassay intended for the quantitative determination of antibodies to infliximab (ATI) in human serum and plasma. Key features [...]
Intended use:For in vitro diagnostic use. RIDASCREEN® ADM Monitoring is an enzyme immunoassay for the quantitative determination of adalimumab (ADM, Humira®) in human serum and plasma. [...]
Intended use:For in-vitro diagnostic use. RIDA®GENE STI Mycoplasma Panel is a multiplex real-time PCR for the direct, qualitative detection of Mycoplasma hominis, Mycoplasma genitalium and [...]
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 [...]
Intended use:For in vitro diagnostic use. This test is an enzyme linked immunoassay intended for the quantitative determination of infliximab (IFX, Remicade®) and the biosimilars Remsima®, [...]
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 [...]