Rapid test for qualitative immunochromatographic determination of fetal fibronectin in cervical secretions "fFN-IMBIAN-IHA" according to TU 21.20.23-119-39271034-2023 In versions: I. Set 1: 1. Test cassette - 1 pc. 2. Buffer solution, 0.5 ml - 1 pc. 3. MiniMed sterile swab probe TU 32.50.50-034-29508133-2020, consisting of: plastic probe (polypropylene), cotton swab, length: 150 mm (RU No RZN 2021/15079) - 1 pc. 4. Instructions for use - 1 pc. 5. Passport - 1 pc. (provided as part of the supply for each series of the product). II. Set 2: 1. Test cassette - 25 pcs. 2. Buffer solution, 0.5 ml - 25 pcs. 3. Sterile MiniMed Sterile Tampon TU 32.50.50-034-29508133-2020, consisting of: plastic probe (polypropylene), cotton swab, length: 150 mm (RU No RZN 2021/15079) - 25 pcs. 4. Instructions for use - 1 pc. 5. Passport - 1 pc. (provided as part of the supply for each series of the product). - Roszdravnadzor Registration РЗН 2024/22722
Access comprehensive regulatory information for Rapid test for qualitative immunochromatographic determination of fetal fibronectin in cervical secretions "fFN-IMBIAN-IHA" according to TU 21.20.23-119-39271034-2023 In versions: I. Set 1: 1. Test cassette - 1 pc. 2. Buffer solution, 0.5 ml - 1 pc. 3. MiniMed sterile swab probe TU 32.50.50-034-29508133-2020, consisting of: plastic probe (polypropylene), cotton swab, length: 150 mm (RU No RZN 2021/15079) - 1 pc. 4. Instructions for use - 1 pc. 5. Passport - 1 pc. (provided as part of the supply for each series of the product). II. Set 2: 1. Test cassette - 25 pcs. 2. Buffer solution, 0.5 ml - 25 pcs. 3. Sterile MiniMed Sterile Tampon TU 32.50.50-034-29508133-2020, consisting of: plastic probe (polypropylene), cotton swab, length: 150 mm (RU No RZN 2021/15079) - 25 pcs. 4. Instructions for use - 1 pc. 5. Passport - 1 pc. (provided as part of the supply for each series of the product). 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 2024/22722 and manufactured by IMBIAN LLC. The device was registered on May 27, 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.

