Reagent for the determination of prothrombin time in blood plasma (THROMBOPLASTIN-AUTO DDS) according to TU 21.20.23.110-209-48813770-2023 Options: I. Option 1: 1. Thromboplastin-AUTO DCS - 10 vials (4.0 ml each). 2. Thromboplastin-AUTO DCS - 10 vials (8.0 ml each). II. Option 2: 1. Thromboplastin-AUTO DCS - 10 vials (4.0 ml each). 1.1. Identification card - 1 piece. 2. Thromboplastin-AUTO DCS - 10 vials (8.0 ml each). 2.2. Identification card - 1 piece. - Roszdravnadzor Registration РЗН 2024/23267

Access comprehensive regulatory information for Reagent for the determination of prothrombin time in blood plasma (THROMBOPLASTIN-AUTO DDS) according to TU 21.20.23.110-209-48813770-2023 Options: I. Option 1: 1. Thromboplastin-AUTO DCS - 10 vials (4.0 ml each). 2. Thromboplastin-AUTO DCS - 10 vials (8.0 ml each). II. Option 2: 1. Thromboplastin-AUTO DCS - 10 vials (4.0 ml each). 1.1. Identification card - 1 piece. 2. Thromboplastin-AUTO DCS - 10 vials (8.0 ml each). 2.2. Identification card - 1 piece. 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 2024/23267 and manufactured by JSC "DIAKON-DS". The device was registered on August 01, 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.