Reagents, reagents for clinical laboratory research: a set of reagents for the detection of Mycoplasma pneumoniae and Chlamydophila pneumoniae DNA in biological material by polymerase chain reaction (PCR) with hybridization-fluorescence detection "AmpliSense® Mycoplasma pneumoniae / Chlamydophila pneumoniae-FL" according to TU 9398-176-01897593-2012 (FEP format, form 6) - Belarus Medical Device Registration

Access comprehensive regulatory information for Reagents, reagents for clinical laboratory research: a set of reagents for the detection of Mycoplasma pneumoniae and Chlamydophila pneumoniae DNA in biological material by polymerase chain reaction (PCR) with hybridization-fluorescence detection "AmpliSense® Mycoplasma pneumoniae / Chlamydophila pneumoniae-FL" according to TU 9398-176-01897593-2012 (FEP format, form 6) in the Belarus medical device market through Pure Global AI's free database. This Medical devices medical device is manufactured by Central Research Institute of Epidemiology of the Federal Service for Surveillance on Consumer Rights Protection and Human Welfare (Central Research Institute of Epidemiology of Rospotrebnadzor). The device was registered on June 21, 2022.

This page provides complete registration details including manufacturer information, product type classification, authorized representative details, and regulatory compliance data from the official Belarus medical device database. Pure Global AI offers free access to Belarus's medical device registry, helping global MedTech companies navigate Belarus regulations efficiently.