"Reagent kit for the quantitative determination of class M antibodies to β2-glycoprotein 1 by enzyme-linked immunosorbent assay ("DS-ELISA-ANTI-β2-GLYCOPROTEIN 1-M") according to TU 21.20.23-246-05941003-2022 Composed of: - Immunosorbent - 96-well collapsible polystyrene plate (up to the wells), In the wells of which purified β2-glycoprotein 1 is sorbed, it is ready for use: 1 tablet. - Human IgM antibody conjugate, labeled with horseradish peroxidase, ready for use: 1 vial. 12.0 ml. - K+ - control positive sample, ready for use: 1 fl. 1.2 ml. - K- - control negative sample, ready for use: 1 fl. 2.5 ml. - Calibrators - calibrators containing known amounts of class M antibodies to β2-glycoprotein 1, ready for use: Calibrator 0 - 1 fl. 1.0 ml, Calibrator 1 - 1 fl. 1.0 ml, Calibrator 2 - 1 vial. 1.0 ml, Calibrator 3 - 1 vial. 1.0 ml, Calibrator 4 - 1 vial. 1.0 ml, Calibrator 5 - 1 vial. 1.0 ml. - BR - block solution for diluting serums, ready for use: 1 bottle. 12.5 ml. - PPC - solution for preliminary dilution of serums, ready for use: 1 fl. 12.5 ml. - PR - flushing solution, concentrate (×25) of phosphate-saline buffer solution with twin (FSB-T): 1 fl. 50.0 ml. - Stop-reagent - sulfuric acid solution (0.2M), ready for use: 1 vial. 25.0 ml. - TMB-Substrate solution, ready to use: 1 fl. 14.0 ml. - Tablet for pre-dilution of serums: 1 tablet. - protective film for ELISA tablets: 2 pcs. - Disposable tips: 16 pcs. - Plastic bath for liquid reagents: 2 pcs. - plastic bag with Zip-Lock: 1 pc. - Calibration graph form: 1 pc. - Instructions for use: 1 pc. - Roszdravnadzor Registration РЗН 2023/19397
Access comprehensive regulatory information for "Reagent kit for the quantitative determination of class M antibodies to β2-glycoprotein 1 by enzyme-linked immunosorbent assay ("DS-ELISA-ANTI-β2-GLYCOPROTEIN 1-M") according to TU 21.20.23-246-05941003-2022 Composed of: - Immunosorbent - 96-well collapsible polystyrene plate (up to the wells), In the wells of which purified β2-glycoprotein 1 is sorbed, it is ready for use: 1 tablet. - Human IgM antibody conjugate, labeled with horseradish peroxidase, ready for use: 1 vial. 12.0 ml. - K+ - control positive sample, ready for use: 1 fl. 1.2 ml. - K- - control negative sample, ready for use: 1 fl. 2.5 ml. - Calibrators - calibrators containing known amounts of class M antibodies to β2-glycoprotein 1, ready for use: Calibrator 0 - 1 fl. 1.0 ml, Calibrator 1 - 1 fl. 1.0 ml, Calibrator 2 - 1 vial. 1.0 ml, Calibrator 3 - 1 vial. 1.0 ml, Calibrator 4 - 1 vial. 1.0 ml, Calibrator 5 - 1 vial. 1.0 ml. - BR - block solution for diluting serums, ready for use: 1 bottle. 12.5 ml. - PPC - solution for preliminary dilution of serums, ready for use: 1 fl. 12.5 ml. - PR - flushing solution, concentrate (×25) of phosphate-saline buffer solution with twin (FSB-T): 1 fl. 50.0 ml. - Stop-reagent - sulfuric acid solution (0.2M), ready for use: 1 vial. 25.0 ml. - TMB-Substrate solution, ready to use: 1 fl. 14.0 ml. - Tablet for pre-dilution of serums: 1 tablet. - protective film for ELISA tablets: 2 pcs. - Disposable tips: 16 pcs. - Plastic bath for liquid reagents: 2 pcs. - plastic bag with Zip-Lock: 1 pc. - Calibration graph form: 1 pc. - Instructions for use: 1 pc. in the Russia medical device market through Pure Global AI's free database. This Class 2a medical device is registered under Roszdravnadzor registration number РЗН 2023/19397 and manufactured by LLC "NPO "Diagnostic Systems". The device was registered on January 24, 2023.
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.

