Anti-Snoring devices - EUDAMED Registration 19330944001312

Access comprehensive regulatory information for Anti-Snoring devices 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 19330944001312 and manufactured by Myofunctional Research Co. in Australia.

This page provides complete registration details including trade name (Myosa KS2), 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.