XMark - EUDAMED Registration 05056256109849

Access comprehensive regulatory information for XMark 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 05056256109849 and manufactured by CellPath Ltd in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (XMARK - TISSUE MARKING DYE - MAGENTA - 250ML BOTTLE), 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.