Durawave - PMDA ID 780226_22800BZX00404000_A_02_02

Access comprehensive regulatory information for Durawave (デュラウェーブ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 780226_22800BZX00404000_A_02_02 and manufactured by Manufacturing and sales: Gunze Medical Corporation. The device information was last updated on October 01, 2024.

This page provides complete registration details including device class (B0400), classification (Synthetic artificial hard membrane / 合成人工硬膜), 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.