Midmark 630 HumanForm Procedure Chair - EUDAMED Registration 00841709116940

Access comprehensive regulatory information for Midmark 630 HumanForm Procedure Chair 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 00841709116940 and manufactured by Midmark Corporation in United States.

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