Deficient plasma by coagulation factor for coagulometers "Technology Solution" (TS-Deficient plasma) according to TU 21.20.23-120-42349142-2023 In versions: I. Variant 1. 1. Deficient plasma by coagulation factor II (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. II. Variant 2. 1. Deficient plasma by coagulation factor V (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. III. Variant 3. 1. Deficient plasma by coagulation factor VII (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. IV. Variant 4. 1. Deficient plasma by coagulation factor X (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. V. Variant 5. 1. Deficient plasma by coagulation factor XI (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. VI. Variant 6. 1. Deficient plasma by coagulation factor XII (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. - Roszdravnadzor Registration РЗН 2023/21757

Access comprehensive regulatory information for Deficient plasma by coagulation factor for coagulometers "Technology Solution" (TS-Deficient plasma) according to TU 21.20.23-120-42349142-2023 In versions: I. Variant 1. 1. Deficient plasma by coagulation factor II (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. II. Variant 2. 1. Deficient plasma by coagulation factor V (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. III. Variant 3. 1. Deficient plasma by coagulation factor VII (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. IV. Variant 4. 1. Deficient plasma by coagulation factor X (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. V. Variant 5. 1. Deficient plasma by coagulation factor XI (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. VI. Variant 6. 1. Deficient plasma by coagulation factor XII (lyophilically dried), per 1 ml - 3 vials. 2. Instructions for use. 3. Passport. 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 2023/21757 and manufactured by Technologia-Standard LLC. The device was registered on December 20, 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.