Japan PMDA registration 790130_13B3X10305THZ003_A_01_01

GSK Knot Pusher

JP: GSK ノットプッシャー
Japan flagJapan·MD·A2500·Updated January 19, 2022
Intended use / 使用目的
English
Refers to an instrument used to join internal wounds by intertwining the ends of sutures with each other during endoscopic treatment. It is a thread knotting device.
日本語 (Japanese)
内視鏡治療時に、縫合糸の末端同士を絡み合わせることによって内部創を結合するために用いる器具をいう。糸結び器である。
Device classification / 分類
Device Type
MD
Device Class
A2500
Class Name (English)
endoscopic ligature
Class Name (日本語)
内視鏡用結さつ器具
Registration information / 登録情報
PMDA ID
790130_13B3X10305THZ003_A_01_01
Last Update Date
January 19, 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 GSK Knot Pusher (GSK ノットプッシャー) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 790130_13B3X10305THZ003_A_01_01 and manufactured by Manufacture and sales/Sunmedics Co., Ltd.. The device information was last updated on January 19, 2022.

This page provides complete registration details including device class (A2500), classification (endoscopic ligature / 内視鏡用結さつ器具), 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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