Japan PMDA registration 370077_222AKBZX00098000_A_01_07

Klinpro Sealant

JP: クリンプロ　シーラント

Japan·MD·C0500·Updated October 01, 2024

Device classification / 分類

Device Type: MD
Device Class: C0500
Class Name (English): Polymer dental foveolar fissure blockade
Class Name (日本語): 高分子系歯科小窩裂溝封鎖材

Registration information / 登録情報

PMDA ID: 370077_222AKBZX00098000_A_01_07
Last Update Date: October 01, 2024
Official Documents: View PDF (PMDA)

Manufacturer / 製造販売業者

English: Manufacturing and sales: 3M Japan Innovation Co., Ltd.
日本語 (Japanese): 製造販売／スリーエムジャパンイノベーション株式会社

About this record

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.

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