Japan PMDA registration 340216_30200BZX00391000_A_01_03

Enseal X1 tissue sealer

JP: エンシール X1 ティシューシーラー
Japan flagJapan·MD·A2900·Updated October 17, 2022
Device classification / 分類
Device Type
MD
Device Class
A2900
Class Name (English)
Active Devices for Therapy
Class Name (日本語)
治療用能動器具
Registration information / 登録情報
PMDA ID
340216_30200BZX00391000_A_01_03
Last Update Date
October 17, 2022
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/ジョンソン・エンド・ジョンソン株式会社
About this record

Access comprehensive regulatory information for Enseal X1 tissue sealer (エンシール X1 ティシューシーラー) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 340216_30200BZX00391000_A_01_03 and manufactured by Johnson & Johnson K.K.. The device information was last updated on October 17, 2022.

This page provides complete registration details including device class (A2900), classification (Active Devices for Therapy / 治療用能動器具), 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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