Japan PMDA registration 112428_25B1X10004000344_A_01_01

スプーンエレバ

JP: スプーンエレバ
Japan flagJapan·MD·A5800·Updated February 04, 2025
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
112428_25B1X10004000344_A_01_01
Last Update Date
February 04, 2025
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/株式会社ACTYPower
About this record

Access comprehensive regulatory information for スプーンエレバ (スプーンエレバ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 112428_25B1X10004000344_A_01_01 and manufactured by ACTYPower Inc.. The device information was last updated on February 04, 2025.

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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