Nelaton catheter - EUDAMED Registration 36975946801101

Access comprehensive regulatory information for Nelaton catheter 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 36975946801101 and manufactured by Changzhou Weite Medical Equipment Co.,Ltd. in China.

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