Multi-Patient Syringe System - EUDAMED Registration 06945764407419

Access comprehensive regulatory information for Multi-Patient Syringe System 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 06945764407419 and manufactured by Shenzhen Antmed Co., Ltd in China.

This page provides complete registration details including trade name (Multi-Patient Syringe System), manufacturer information, authorized representative details, competent authority (DE/CA22 - Bezirksregierung Münster), 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.