Reagent kit for detection and differentiation of hepatitis C virus (HCV) genotypes in clinical material by polymerase chain reaction (PCR) with hybridization-fluorescence detection in "real time" "AmpliSens® HCV-genotype-FL" Forms of configuration: I. Form 3: "PCR kit" version FRT-g1-4, consisting of: 1. PCR mixture-1-FRT HCV genotypes 1b/3a - 0.6 ml x 1. 2. PCR mixture-1-FRT HCV genotypes 1a/2 - 0.6 ml x 1. 3. PCR mixture-1-FRT HCV VKO/genotype 4 - 0.6 ml x 1. 4. PCR buffer-C - 0.3 ml x 3. 5. Polymerase (TaqF) - 0.03 ml x 3. 6. PCO cDNA HCV genotypes 1b/3a - 0.2 ml x 1. 7. PCO cDNA HCV genotypes 1a/2 - 0.2 ml x 1. 8. PCP cDNA HCV/genotype 4 - 0.2 ml x 1. 9. K- - 0.5 ml x 1. 10. OKO - 1.2 ml x 1. 11. VKO STI-248-rec - 0.5 ml x 1. 12. 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 guide to the reagent kit - 1 pc. II. Form 6: "PCR kit" version FRT-g1-6, consisting of: 1. PCR mixture-1-FRT HCV genotypes 1b/3a - 0.6 ml x 1. 2. PCR mixture-1-FRT HCV genotypes 1a/2 - 0.6 ml x 1. 3. PCR mixture-1-FRT HCV VKO/genotype 4 - 0.6 ml x 1. 4. PCR mixture-1-FRT HCV genotypes 5a/6 - 0.6 ml x 1. 5. PCR-buffer-C - 0.3 ml x 4. 6. Polymerase (TaqF) - 0.03 ml x 4. 7. PCO cDNA HCV genotypes 1b/3a - 0.2 ml x 1. 8. PCO cDNA HCV genotypes 1a/2 - 0.2 ml x 1. 9. PCO cDNA HCV/genotype 4 - 0.2 ml x 1. 10. PCO cDNA HCV genotypes 5a/6 - 0.2 ml x 1. 11. K- - 0.5 ml x 1. 12. OKO - 1.2 ml x 1. 13. VKO STI-248-rec - 0.5 ml x 1. 14. 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 guide to the reagent kit - 1 pc. - Roszdravnadzor Registration ФСР 2012/13048
Access comprehensive regulatory information for Reagent kit for detection and differentiation of hepatitis C virus (HCV) genotypes in clinical material by polymerase chain reaction (PCR) with hybridization-fluorescence detection in "real time" "AmpliSens® HCV-genotype-FL" Forms of configuration: I. Form 3: "PCR kit" version FRT-g1-4, consisting of: 1. PCR mixture-1-FRT HCV genotypes 1b/3a - 0.6 ml x 1. 2. PCR mixture-1-FRT HCV genotypes 1a/2 - 0.6 ml x 1. 3. PCR mixture-1-FRT HCV VKO/genotype 4 - 0.6 ml x 1. 4. PCR buffer-C - 0.3 ml x 3. 5. Polymerase (TaqF) - 0.03 ml x 3. 6. PCO cDNA HCV genotypes 1b/3a - 0.2 ml x 1. 7. PCO cDNA HCV genotypes 1a/2 - 0.2 ml x 1. 8. PCP cDNA HCV/genotype 4 - 0.2 ml x 1. 9. K- - 0.5 ml x 1. 10. OKO - 1.2 ml x 1. 11. VKO STI-248-rec - 0.5 ml x 1. 12. 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 guide to the reagent kit - 1 pc. II. Form 6: "PCR kit" version FRT-g1-6, consisting of: 1. PCR mixture-1-FRT HCV genotypes 1b/3a - 0.6 ml x 1. 2. PCR mixture-1-FRT HCV genotypes 1a/2 - 0.6 ml x 1. 3. PCR mixture-1-FRT HCV VKO/genotype 4 - 0.6 ml x 1. 4. PCR mixture-1-FRT HCV genotypes 5a/6 - 0.6 ml x 1. 5. PCR-buffer-C - 0.3 ml x 4. 6. Polymerase (TaqF) - 0.03 ml x 4. 7. PCO cDNA HCV genotypes 1b/3a - 0.2 ml x 1. 8. PCO cDNA HCV genotypes 1a/2 - 0.2 ml x 1. 9. PCO cDNA HCV/genotype 4 - 0.2 ml x 1. 10. PCO cDNA HCV genotypes 5a/6 - 0.2 ml x 1. 11. K- - 0.5 ml x 1. 12. OKO - 1.2 ml x 1. 13. VKO STI-248-rec - 0.5 ml x 1. 14. 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 guide to the reagent kit - 1 pc. in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number ФСР 2012/13048 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.

