Endotracheal Tube - EUDAMED Registration D-ETT5013CHG

Access comprehensive regulatory information for Endotracheal Tube in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI D-ETT5013CHG and manufactured by Hangzhou Tappa Medical Technology Co , Ltd. in China.

This page provides complete registration details including trade name (Endotracheal Tube), manufacturer information, authorized representative details, competent authority (DE/CA20, Bezirksregierung Düsseldorf Dezernat 24), 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.