RIDA®GENE STI Mycoplasma Panel
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 [...]
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 STI Mycoplasma Panel is a multiplex real-time PCR for the direct, qualitative detection of Mycoplasma hominis, Mycoplasma genitalium and [...]