Reagent kit for the detection of Chlamydia trachomatis DNA in clinical material by polymerase chain reaction (PCR) with hybridization-fluorescence detection "AmpliSense® Chlamydia trachomatis-FL" Forms of configuration: FEP Format Form 1: "PCR kit" version FEP (0.5 ml tubes), consisting of: 1. PCR mixture-1-FL Chlamydia trachomatis - 110 tubes (0.01 ml). 2. PCR mixture-2-FL-red - 1 tube (1.1 ml). 3. PCR-mixture-Fon-red - 1 tube (0.6 ml). 4. Mineral oil for PCR - 1 vial (4.0 ml). 5. Complex PCS - 1 tube (0.2 ml). 6. DNA buffer - 1 tube (0.5 ml). 7. Operational documentation on paper and on the website of the Manufacturer (authorized representative): 8. Instructions for use - 1 pc. 9. Quality certificate of the reagent kit - 1 pc. 10. Insert for the reagent kit - 1 set. 11. Quick guide to the reagent kit - 1 pc. Form 2: "PCR kit" version FEP (0.2 ml tubes), consisting of: 1. PCR mixture-1-FL Chlamydia trachomatis - 110 tubes (0.01 ml). 2. PCR mixture-2-FL-red - 1 tube (1.1 ml). 3. PCR-mixture-Fon-red - 1 tube (0.6 ml). 4. Complex PCS - 1 tube (0.2 ml). 5. DNA buffer - 1 tube (0.5 ml). 6. Operational documentation on paper and on the website of the Manufacturer (authorized representative): 7. Instructions for use - 1 pc. 8. Quality passport of the reagent kit - 1 pc. 9. Insert for the reagent kit - 1 set. 10. Quick guide to the reagent kit - 1 pc. FRT Format Form 1: "PCR kit" version FRT, consisting of: 1. PCR mixture-1-FL Chlamydia trachomatis - 110 tubes (0.01 ml). 2. PCR mixture-2-FL-red - 1 tube (1.1 ml). 3. Complex PCS - 1 tube (0.2 ml). 4. DNA buffer - 1 tube (0.5 ml). 5. Software on electronic media or on the website of the Manufacturer (authorized representative): 6. Software AmpliSens® Chlamydia trachomatis Soft Form 1 version 1 - 1 pc. 7. Operator's manual - 1 pc. 8. Operational documentation on paper and on the website of the Manufacturer (authorized representative): 9. Instructions for use - 1 pc. 10. Quality certificate of the reagent kit - 1 pc. 11. Insert for the reagent kit - 1 set. 12. Quick guide to the reagent kit - 1 pc. Form 2: "PCR kit" version FRT-100 F, consisting of: 1. PCR mixture-1-FL Chlamydia trachomatis - 1 tube (1.2 ml). 2. PCR mixture-2-FRT - 2 tubes (0.3 ml). 3. Polymerase (TaqF) - 2 tubes (0.03 ml). 4. Complex PCS - 1 tube (0.2 ml). 5. DNA buffer - 1 tube (0.5 ml). 6. Software on electronic media or on the website of the Manufacturer (authorized representative): 7. Software AmpliSens® Chlamydia trachomatis Soft Form 2 version 1 - 1 pc. 8. Operator's manual - 1 pc. 9. Operational documentation on paper and on the website of the Manufacturer (authorized representative): 10. Instructions for use - 1 pc. 11. Quality certificate of the reagent kit - 1 pc. 12. Insert for the reagent kit - 1 set. 13. Quick guide to the reagent kit - 1 pc. - Roszdravnadzor Registration ФСР 2009/06555
Access comprehensive regulatory information for Reagent kit for the detection of Chlamydia trachomatis DNA in clinical material by polymerase chain reaction (PCR) with hybridization-fluorescence detection "AmpliSense® Chlamydia trachomatis-FL" Forms of configuration: FEP Format Form 1: "PCR kit" version FEP (0.5 ml tubes), consisting of: 1. PCR mixture-1-FL Chlamydia trachomatis - 110 tubes (0.01 ml). 2. PCR mixture-2-FL-red - 1 tube (1.1 ml). 3. PCR-mixture-Fon-red - 1 tube (0.6 ml). 4. Mineral oil for PCR - 1 vial (4.0 ml). 5. Complex PCS - 1 tube (0.2 ml). 6. DNA buffer - 1 tube (0.5 ml). 7. Operational documentation on paper and on the website of the Manufacturer (authorized representative): 8. Instructions for use - 1 pc. 9. Quality certificate of the reagent kit - 1 pc. 10. Insert for the reagent kit - 1 set. 11. Quick guide to the reagent kit - 1 pc. Form 2: "PCR kit" version FEP (0.2 ml tubes), consisting of: 1. PCR mixture-1-FL Chlamydia trachomatis - 110 tubes (0.01 ml). 2. PCR mixture-2-FL-red - 1 tube (1.1 ml). 3. PCR-mixture-Fon-red - 1 tube (0.6 ml). 4. Complex PCS - 1 tube (0.2 ml). 5. DNA buffer - 1 tube (0.5 ml). 6. Operational documentation on paper and on the website of the Manufacturer (authorized representative): 7. Instructions for use - 1 pc. 8. Quality passport of the reagent kit - 1 pc. 9. Insert for the reagent kit - 1 set. 10. Quick guide to the reagent kit - 1 pc. FRT Format Form 1: "PCR kit" version FRT, consisting of: 1. PCR mixture-1-FL Chlamydia trachomatis - 110 tubes (0.01 ml). 2. PCR mixture-2-FL-red - 1 tube (1.1 ml). 3. Complex PCS - 1 tube (0.2 ml). 4. DNA buffer - 1 tube (0.5 ml). 5. Software on electronic media or on the website of the Manufacturer (authorized representative): 6. Software AmpliSens® Chlamydia trachomatis Soft Form 1 version 1 - 1 pc. 7. Operator's manual - 1 pc. 8. Operational documentation on paper and on the website of the Manufacturer (authorized representative): 9. Instructions for use - 1 pc. 10. Quality certificate of the reagent kit - 1 pc. 11. Insert for the reagent kit - 1 set. 12. Quick guide to the reagent kit - 1 pc. Form 2: "PCR kit" version FRT-100 F, consisting of: 1. PCR mixture-1-FL Chlamydia trachomatis - 1 tube (1.2 ml). 2. PCR mixture-2-FRT - 2 tubes (0.3 ml). 3. Polymerase (TaqF) - 2 tubes (0.03 ml). 4. Complex PCS - 1 tube (0.2 ml). 5. DNA buffer - 1 tube (0.5 ml). 6. Software on electronic media or on the website of the Manufacturer (authorized representative): 7. Software AmpliSens® Chlamydia trachomatis Soft Form 2 version 1 - 1 pc. 8. Operator's manual - 1 pc. 9. Operational documentation on paper and on the website of the Manufacturer (authorized representative): 10. Instructions for use - 1 pc. 11. Quality certificate of the reagent kit - 1 pc. 12. Insert for the reagent kit - 1 set. 13. Quick guide to the 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 ФСР 2009/06555 and manufactured by Central Research Institute of Epidemiology of Rospotrebnadzor. The device was registered on May 30, 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.

