Japan PMDA registration 750054_13B1X00306G10896_C_01_05

Multi-Purpose Headframe II (Multi-Purpose Headframe II Frameset)

JP: 多目的ヘッドフレームII(多目的ヘッドフレームIIフレームセット)
Japan flagJapan·MD·A3900·Updated August 15, 2024
Device classification / 分類
Device Type
MD
Device Class
A3900
Class Name (English)
Head surgery clamp
Class Name (日本語)
頭部手術用クランプ
Registration information / 登録情報
PMDA ID
750054_13B1X00306G10896_C_01_05
Last Update Date
August 15, 2024
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/ミズホ株式会社
About this record

Access comprehensive regulatory information for Multi-Purpose Headframe II (Multi-Purpose Headframe II Frameset) (多目的ヘッドフレームII(多目的ヘッドフレームIIフレームセット)) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 750054_13B1X00306G10896_C_01_05 and manufactured by Manufacturing and sales: Mizuho Corporation. The device information was last updated on August 15, 2024.

This page provides complete registration details including device class (A3900), classification (Head surgery clamp / 頭部手術用クランプ), 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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