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bone forceps KR - PMDA ID 341095_17B2X10001000016_A_01_03

骨鉗子KR

Access comprehensive regulatory information for bone forceps KR (骨鉗子KR) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 341095_17B2X10001000016_A_01_03 and manufactured by Dental Medical Co., Ltd.. The device information was last updated on January 30, 2025.

This page provides complete registration details including device class (A3900), classification (Dental bone forceps / 歯科用骨鉗子), 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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MD
A3900
341095_17B2X10001000016_A_01_03
MD
A3900
bone forceps KR
骨鉗子KR
PMDA ID: 341095_17B2X10001000016_A_01_03
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Device Classification / 分類
Device Type
MD
Device Class
A3900
Class Name (English)
Dental bone forceps
Class Name (日本語)
歯科用骨鉗子
Registration Information / 登録情報
PMDA ID
341095_17B2X10001000016_A_01_03
Last Update Date
January 30, 2025
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/株式会社 歯愛メディカル
Product Names / 製品名
Market Name (English)
bone forceps KR
Market Name (日本語)
骨鉗子KR