Japan PMDA registration 530366_22700BZX00131000_A_02_07

Pipeline Flex フローダイバーターシステム

JP: Pipeline Flex フローダイバーターシステム
Japan flagJapan·MD·A5100·Updated February 19, 2025
Device classification / 分類
Device Type
MD
Device Class
A5100
Class Name (English)
Prosthesis for promoting central circulatory endovascular embolization
Class Name (日本語)
中心循環系血管内塞栓促進用補綴材
Registration information / 登録情報
PMDA ID
530366_22700BZX00131000_A_02_07
Last Update Date
February 19, 2025
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/日本メドトロニック株式会社
About this record

Access comprehensive regulatory information for Pipeline Flex フローダイバーターシステム (Pipeline Flex フローダイバーターシステム) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530366_22700BZX00131000_A_02_07 and manufactured by Japan Medtronic Corporation. The device information was last updated on February 19, 2025.

This page provides complete registration details including device class (A5100), classification (Prosthesis for promoting central circulatory endovascular embolization / 中心循環系血管内塞栓促進用補綴材), 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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