Swabs Nonwoven, folded, sterile - EUDAMED Registration 06438129170450

Access comprehensive regulatory information for Swabs Nonwoven, folded, sterile 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 06438129170450 and manufactured by OneMed Group Oy in Finland.

This page provides complete registration details including trade name (Embra® Nonwoven swabs 10 x 20 cm, 2-pack, sterile), manufacturer information, competent authority (Finnish Medicines Agency, Supervision and licences, Medical Device Unit), 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.