Dye for cytological studies (Hematoxylin Carazzi) "DIACHEM-CYTOSTEIN-GK" as per TU 9398-059-27428909-2012 In versions: I. Configuration 1, consisting of: - hematoxylin Carazzi - 1 vial (250 ml). The delivery set includes instructions for use and a passport. II. Configuration 2, consisting of: - Hematoxylin Carazzi - 1 vial (1000 ml). The delivery set includes instructions for use and a passport. - Roszdravnadzor Registration ФСР 2012/14184

Access comprehensive regulatory information for Dye for cytological studies (Hematoxylin Carazzi) "DIACHEM-CYTOSTEIN-GK" as per TU 9398-059-27428909-2012 In versions: I. Configuration 1, consisting of: - hematoxylin Carazzi - 1 vial (250 ml). The delivery set includes instructions for use and a passport. II. Configuration 2, consisting of: - Hematoxylin Carazzi - 1 vial (1000 ml). The delivery set includes instructions for use and a 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 ФСР 2012/14184 and manufactured by NPF ABRIS+ LLC. The device was registered on February 28, 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.