Sliding Hammer - EUDAMED Registration D-CNMF0000201150709J2

Access comprehensive regulatory information for Sliding Hammer 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 D-CNMF0000201150709J2 and manufactured by Tianjin Zhengtian Medical Instrument Co., Ltd. in China.

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA39, Regierungspräsidium Freiburg Referat 25), 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.