Reagent kit for qualitative and quantitative determination of Mycoplasma genitalium DNA in human biological material by PCR with "real-time" detection (Amplitech MG (R)) according to TU 21.20.23-031-19926214-2023 Composed of: 1. Tablet with MG(R) Mixture - 1 pc. 2. Films for the tablet - 2 pcs. 3. OK - 0.8 ml x 1 tube. 4. PC U - 0.8 ml x 1 tube. 5. Instructions for use - 1 pc. in paper form and in electronic form at the address: http://www.amplitech.ru/resources/. 6. Quick Start Guide - 1 pc in paper form. 7. Passport - 1 pc. in electronic form at the address: http://www.amplitech.ru/quality/. - Roszdravnadzor Registration РЗН 2024/22780

Access comprehensive regulatory information for Reagent kit for qualitative and quantitative determination of Mycoplasma genitalium DNA in human biological material by PCR with "real-time" detection (Amplitech MG (R)) according to TU 21.20.23-031-19926214-2023 Composed of: 1. Tablet with MG(R) Mixture - 1 pc. 2. Films for the tablet - 2 pcs. 3. OK - 0.8 ml x 1 tube. 4. PC U - 0.8 ml x 1 tube. 5. Instructions for use - 1 pc. in paper form and in electronic form at the address: http://www.amplitech.ru/resources/. 6. Quick Start Guide - 1 pc in paper form. 7. Passport - 1 pc. in electronic form at the address: http://www.amplitech.ru/quality/. in the Russia medical device market through Pure Global AI's free database. This Class 2b medical device is registered under Roszdravnadzor registration number РЗН 2024/22780 and manufactured by LLC "Amplitek". The device was registered on May 29, 2024.

This page provides complete registration details including device type, manufacturer information, country of origin (Russia), and regulatory compliance data from the official Russia Roszdravnadzor medical device database. Pure Global AI offers free access to Russia's complete medical device registry, helping global MedTech companies navigate Roszdravnadzor regulations efficiently.