Protection/Examination Sheet - EUDAMED Registration 06973911697604

Access comprehensive regulatory information for Protection/Examination Sheet 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 06973911697604 and manufactured by Finess Healthcare Group Co.,Ltd in China.

This page provides complete registration details including trade name (PE beschichtet - Tissue), manufacturer information, authorized representative details, competent authority (Agencia Española de Medicamentos y Productos Sanitarios), 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.