GLUCOCARD S onyx (GT-7120) - EUDAMED Registration D-109323MW

Access comprehensive regulatory information for GLUCOCARD S onyx (GT-7120) in the European Union medical device market through Pure Global AI's free database. This IVD Annex II List B device is registered with EU EUDAMED under Primary DI D-109323MW and manufactured by ARKRAY Factory, Inc. in Japan.

This page provides complete registration details including trade name (GLUCOCARD S onyx (GT-7120)), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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.