Chlamydia Trachomatis Test - EUDAMED Registration 06941571816017

Access comprehensive regulatory information for Chlamydia Trachomatis Test in the European Union medical device market through Pure Global AI's free database. This IVD Annex II List B device is registered with EU EUDAMED under Primary DI 06941571816017 and manufactured by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd. in China.

This page provides complete registration details including 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.