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vertebral arch spacer B-16-KS series trial - PMDA ID 784801_22B1X10004M00356_A_01_01

椎弓スペーサー B−16−KS シリーズトライアル

Access comprehensive regulatory information for vertebral arch spacer B-16-KS series trial (椎弓スペーサー B−16−KS シリーズトライアル) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 784801_22B1X10004M00356_A_01_01 and manufactured by Mext Corporation. The device information was last updated on September 25, 2024.

This page provides complete registration details including device class (A5800), classification (Bone surgery instrument / 骨手術用器械), 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
Bilingual (EN/JP)
MD
A5800
784801_22B1X10004M00356_A_01_01
MD
A5800
vertebral arch spacer B-16-KS series trial
椎弓スペーサー B−16−KS シリーズトライアル
PMDA ID: 784801_22B1X10004M00356_A_01_01
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Device Classification / 分類
Device Type
MD
Device Class
A5800
Class Name (English)
Bone surgery instrument
Class Name (日本語)
骨手術用器械
Registration Information / 登録情報
PMDA ID
784801_22B1X10004M00356_A_01_01
Last Update Date
September 25, 2024
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/株式会社メクスト
Product Names / 製品名
Market Name (English)
vertebral arch spacer B-16-KS series trial
Market Name (日本語)
椎弓スペーサー B−16−KS シリーズトライアル