NovoCyte Quanteon Dx Flow Cytometer - EUDAMED Registration 06974501890009

Access comprehensive regulatory information for NovoCyte Quanteon Dx Flow Cytometer in the European Union medical device market through Pure Global AI's free database. This Class A device is registered with EU EUDAMED under Primary DI 06974501890009 and manufactured by Agilent Biosciences (Hangzhou) Co., Ltd. in China.

This page provides complete registration details including trade name (NovoCyte Quanteon Dx Flow Cytometer), manufacturer information, authorized representative details, competent authority (The Medicines and Healthcare Products Regulatory Agency), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.