Biopsy Guidance - EUDAMED Registration 00884838118478

Access comprehensive regulatory information for Biopsy Guidance 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 00884838118478 and manufactured by Invivo Corporation in United States.

This page provides complete registration details including trade name (Fiducial Marker Grid Block Assembly), 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.