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Heart Start Intrepid - PMDA ID 670277_30300BZX00239000_A_01_02

ハートスタート Intrepid

Access comprehensive regulatory information for Heart Start Intrepid (ハートスタート Intrepid) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 670277_30300BZX00239000_A_01_02 and manufactured by Philips Japan Co., Ltd.. The device information was last updated on July 01, 2022.

This page provides complete registration details including device class (A1200), classification (manual fine mover / 手動式除細動器), manufacturer information (English and Japanese), intended use, 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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PMDA Official Data
Bilingual (EN/JP)
MD
A1200
670277_30300BZX00239000_A_01_02
MD
A1200
Heart Start Intrepid
ハートスタート Intrepid
PMDA ID: 670277_30300BZX00239000_A_01_02
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Intended Use / 使用目的
English

This product is used for the purpose of performing cardiac defibrillation by supplying an electric pulse shock outside the body or via electrodes inside the body. It also functions as a patient information monitor.

日本語 (Japanese)

本品は、体外又は体内の電極を介して電気パルスショックを供給することによって心臓の除細動を行うことを目的として使用する。また、生体情報モニタとしての機能も備える。

Device Classification / 分類
Device Type
MD
Device Class
A1200
Class Name (English)
manual fine mover
Class Name (日本語)
手動式除細動器
Registration Information / 登録情報
PMDA ID
670277_30300BZX00239000_A_01_02
Last Update Date
July 01, 2022
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/株式会社フィリップス・ジャパン
Product Names / 製品名
Market Name (English)
Heart Start Intrepid
Market Name (日本語)
ハートスタート Intrepid