Klinpro Sealant - PMDA ID 370077_222AKBZX00098000_A_01_07

Access comprehensive regulatory information for Klinpro Sealant (クリンプロ　シーラント) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 370077_222AKBZX00098000_A_01_07 and manufactured by Manufacturing and sales: 3M Japan Innovation Co., Ltd.. The device information was last updated on October 01, 2024.

This page provides complete registration details including device class (C0500), classification (Polymer dental foveolar fissure blockade / 高分子系歯科小窩裂溝封鎖材), 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.