Dental Surgical Instrument - EUDAMED Registration 08800263100545

Access comprehensive regulatory information for Dental Surgical Instrument 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 08800263100545 and manufactured by Neobiotech Co.,Ltd. in Republic of Korea.

This page provides complete registration details including trade name (NeoGuide Vertical Anchor (In Fixture)_Body), 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.