Japan PMDA registration 790130_13B3X10305EG7099_A_01_01

don kelly dissection forceps

JP: ドン・ケリー剥離鉗子
Japan flagJapan·MD·A3900·Updated May 11, 2022
Intended use / 使用目的
English
This product is a surgical instrument used to grip, bind, compress or support an organ, tissue or blood vessel atraumatically. This product can be reused.
日本語 (Japanese)
本 製品は、臓器、組織又は血管を非外傷的に把持、結合、圧迫又は支持するために用いる手術器械である。なお、本品は再使用可能である。
Device classification / 分類
Device Type
MD
Device Class
A3900
Class Name (English)
pliers
Class Name (日本語)
鉗子
Registration information / 登録情報
PMDA ID
790130_13B3X10305EG7099_A_01_01
Last Update Date
May 11, 2022
Official Documents
View PDF (PMDA)
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/サンメディックス株式会社
About this record

Access comprehensive regulatory information for don kelly dissection forceps (ドン・ケリー剥離鉗子) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 790130_13B3X10305EG7099_A_01_01 and manufactured by Manufacture and sales/Sunmedics Co., Ltd.. The device information was last updated on May 11, 2022.

This page provides complete registration details including device class (A3900), classification (pliers / 鉗子), manufacturer information (English and Japanese), intended use, 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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