Reagent kit for qualitative and quantitative determination and differentiation of DNA of papillomaviruses types 6 and 11 in human biological material by PCR with real-time detection (Amplitech HPV 6/11 (R)) according to TU 21.20.23-036-19926214-2023 Composed of: 1. Tablet with HPV 6/11 (R) Mixture - 1 pc. 2. Films for the tablet - 2 pcs. 3. OK - 0.8 ml x 1 tube. 4. PC HPV - 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 2024/22603

Access comprehensive regulatory information for Reagent kit for qualitative and quantitative determination and differentiation of DNA of papillomaviruses types 6 and 11 in human biological material by PCR with real-time detection (Amplitech HPV 6/11 (R)) according to TU 21.20.23-036-19926214-2023 Composed of: 1. Tablet with HPV 6/11 (R) Mixture - 1 pc. 2. Films for the tablet - 2 pcs. 3. OK - 0.8 ml x 1 tube. 4. PC HPV - 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 2024/22603 and manufactured by LLC "Amplitek". The device was registered on May 08, 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.