Reagent kit for the quantitative determination of DNA of human papillomaviruses (HPV) of high carcinogenic risk (HRC) types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 in biological material by polymerase chain reaction (PCR) for in vitro diagnostics "AmpliSens® HPV WRC screen-titr-14-FL" Form 1: "PCR kit" variant FRT-100 FN The kit includes: 1. PCR mixture-FL HPV 14 1.2 ml × 1 pc. 2. PCR-buffer-H 0.6 ml × 1 pc. 3. K1 HPV screen 0.2 ml × 1 pc. 4. K2 HPV screen 0.2 ml × 1 pc. 5. K− 0.2 ml × 1 pc. 6. Electronic calculator on the Manufacturer's website (www.amplisens.ru): - Electronic calculator based on Microsoft® Excel "AmpliSense® HPV Thesis Screen-Titr-14" 1 pc. 7. Operational documentation on paper and on the Manufacturer's website (www.amplisens.ru): - instructions for use 1 pc.; - Quality certificate of the reagent kit 1 pc.; - Insert for the reagent kit 1 set; - Quick Start Guide to Reagent Kit 1 pc. - Roszdravnadzor Registration РЗН 2017/5387
Access comprehensive regulatory information for Reagent kit for the quantitative determination of DNA of human papillomaviruses (HPV) of high carcinogenic risk (HRC) types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 in biological material by polymerase chain reaction (PCR) for in vitro diagnostics "AmpliSens® HPV WRC screen-titr-14-FL" Form 1: "PCR kit" variant FRT-100 FN The kit includes: 1. PCR mixture-FL HPV 14 1.2 ml × 1 pc. 2. PCR-buffer-H 0.6 ml × 1 pc. 3. K1 HPV screen 0.2 ml × 1 pc. 4. K2 HPV screen 0.2 ml × 1 pc. 5. K− 0.2 ml × 1 pc. 6. Electronic calculator on the Manufacturer's website (www.amplisens.ru): - Electronic calculator based on Microsoft® Excel "AmpliSense® HPV Thesis Screen-Titr-14" 1 pc. 7. Operational documentation on paper and on the Manufacturer's website (www.amplisens.ru): - instructions for use 1 pc.; - Quality certificate of the reagent kit 1 pc.; - Insert for the reagent kit 1 set; - Quick Start Guide to Reagent Kit 1 pc. 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 2017/5387 and manufactured by Central Research Institute of Epidemiology of Rospotrebnadzor. The device was registered on August 12, 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.

