EVA NEXUS Pack/Kit - PMDA ID 100707_30500BZI00026000_C_01_01

Access comprehensive regulatory information for EVA NEXUS Pack/Kit (ＥＶＡ　ＮＥＸＵＳ　パック／キット) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 100707_30500BZI00026000_C_01_01 and manufactured by Manufacturing and sales: R E Medical Corporation. The device information was last updated on April 17, 2024.

This page provides complete registration details including device class (A1200), classification (Cataract and vitreous surgery equipment / 白内障・硝子体手術装置), manufacturer information (English and Japanese), and regulatory compliance data from the official Japan PMDA medical device database. Pure Global AI offers free bilingual access to Japan's complete medical device registry, helping global MedTech companies navigate PMDA regulations efficiently.