BULKFLEX ELASTIK - EUDAMED Registration 07798148623443

Access comprehensive regulatory information for BULKFLEX ELASTIK in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 07798148623443 and manufactured by NUXEN SRL in Argentina.

This page provides complete registration details including trade name (BULKFLEX ELASTIK 22 PEQUEÑO EL1 – BF41), manufacturer information, authorized representative details, competent authority (INFARMED - Autoridade Nacional do Medicamento e Produtos de Saúde, I.P.), 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.