Reagent kit for the detection of human cytomegalovirus (CMV) DNA by polymerase chain reaction (CMV-GENE) according to TU 9398-005-46482062-2008 1. PCR with real-time detection: a) Packing S, strips: - Amplification mixture sealed with paraffin - 12 strips of 8 tubes (20 μl each); - Taq polymerase solution - 2 tubes (500 μl each); - Mineral oil - 2 test tubes (1.0 ml each); - Positive control sample - 1 tube (130 μl); Strip lids - 12 pcs. b) Filling S, test tubes: - Amplification mixture sealed with paraffin - 96 tubes (20 μl each); - Taq polymerase solution - 2 tubes (500 μl each); - Mineral oil - 2 test tubes (1.0 ml each); - Positive control sample - 1 tube (130 μL). c) Packing W: Amplification mixture - 2 tubes (1.0 ml each); - Taq polymerase solution - 2 tubes (500 μl each); - Mineral oil - 2 test tubes (1.0 ml each); - Paraffin - 2 tubes (1.0 ml each); - Positive control sample - 1 tube (130 μL). d) Packing U: - Amplification mixture - 1 tube (600 μl); - TexnoTaq MAX polymerase - 1 tube (30 μl); - PCR buffer - 1 tube (600 μl); - Positive control sample - 1 tube (130 μL). 2. PCR with fluorescence endpoint detection: Packaging S: - Amplification mixture sealed with paraffin - 100 tubes (20 μl each); - Taq polymerase solution - 2 tubes (500 μl each); - PCR buffer (background) - 1 tube (200 μl); - Mineral oil - 2 test tubes (1.0 ml each); - Positive control sample - 1 tube (130 μL). 3. PCR with detection by gel electrophoresis: Packaging S: - Amplification mixture sealed with paraffin - 100 tubes (20 μl each); - Taq polymerase solution - 2 tubes (500 μl each); - Mineral oil - 2 test tubes (1.0 ml each); - Positive control sample - 1 tube (130 μL). - Roszdravnadzor Registration ФСР 2008/03945
Access comprehensive regulatory information for Reagent kit for the detection of human cytomegalovirus (CMV) DNA by polymerase chain reaction (CMV-GENE) according to TU 9398-005-46482062-2008 1. PCR with real-time detection: a) Packing S, strips: - Amplification mixture sealed with paraffin - 12 strips of 8 tubes (20 μl each); - Taq polymerase solution - 2 tubes (500 μl each); - Mineral oil - 2 test tubes (1.0 ml each); - Positive control sample - 1 tube (130 μl); Strip lids - 12 pcs. b) Filling S, test tubes: - Amplification mixture sealed with paraffin - 96 tubes (20 μl each); - Taq polymerase solution - 2 tubes (500 μl each); - Mineral oil - 2 test tubes (1.0 ml each); - Positive control sample - 1 tube (130 μL). c) Packing W: Amplification mixture - 2 tubes (1.0 ml each); - Taq polymerase solution - 2 tubes (500 μl each); - Mineral oil - 2 test tubes (1.0 ml each); - Paraffin - 2 tubes (1.0 ml each); - Positive control sample - 1 tube (130 μL). d) Packing U: - Amplification mixture - 1 tube (600 μl); - TexnoTaq MAX polymerase - 1 tube (30 μl); - PCR buffer - 1 tube (600 μl); - Positive control sample - 1 tube (130 μL). 2. PCR with fluorescence endpoint detection: Packaging S: - Amplification mixture sealed with paraffin - 100 tubes (20 μl each); - Taq polymerase solution - 2 tubes (500 μl each); - PCR buffer (background) - 1 tube (200 μl); - Mineral oil - 2 test tubes (1.0 ml each); - Positive control sample - 1 tube (130 μL). 3. PCR with detection by gel electrophoresis: Packaging S: - Amplification mixture sealed with paraffin - 100 tubes (20 μl each); - Taq polymerase solution - 2 tubes (500 μl each); - Mineral oil - 2 test tubes (1.0 ml each); - Positive control sample - 1 tube (130 μL). 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 2008/03945 and manufactured by DNA-Technology TS LLC. The device was registered on August 07, 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.

