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C2−9−Dプローブ(C2−9−Dプローブ/C2−9VN−Dプローブ/C2−9−RSプローブ) - PMDA ID 530979_224ABBZX00142000_A_01_09

C2−9−Dプローブ(C2−9−Dプローブ/C2−9VN−Dプローブ/C2−9−RSプローブ)

Access comprehensive regulatory information for C2−9−Dプローブ(C2−9−Dプローブ/C2−9VN−Dプローブ/C2−9−RSプローブ) (C2−9−Dプローブ(C2−9−Dプローブ/C2−9VN−Dプローブ/C2−9−RSプローブ)) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 530979_224ABBZX00142000_A_01_09 and manufactured by GE Healthcare Japan K.K.. The device information was last updated on October 07, 2024.

This page provides complete registration details including device class (A1200), classification (Hand-heldextracorporeal ultrasound probe / 手持型体外式超音波診断用プローブ), 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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PMDA Official Data
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MD
A1200
530979_224ABBZX00142000_A_01_09
MD
A1200
C2−9−Dプローブ(C2−9−Dプローブ/C2−9VN−Dプローブ/C2−9−RSプローブ)
C2−9−Dプローブ(C2−9−Dプローブ/C2−9VN−Dプローブ/C2−9−RSプローブ)
PMDA ID: 530979_224ABBZX00142000_A_01_09
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Device Classification / 分類
Device Type
MD
Device Class
A1200
Class Name (English)
Hand-heldextracorporeal ultrasound probe
Class Name (日本語)
手持型体外式超音波診断用プローブ
Registration Information / 登録情報
PMDA ID
530979_224ABBZX00142000_A_01_09
Last Update Date
October 07, 2024
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/GEヘルスケア・ジャパン株式会社
Product Names / 製品名
Market Name (English)
C2−9−Dプローブ(C2−9−Dプローブ/C2−9VN−Dプローブ/C2−9−RSプローブ)
Market Name (日本語)
C2−9−Dプローブ(C2−9−Dプローブ/C2−9VN−Dプローブ/C2−9−RSプローブ)