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NOVOSTITCH Meniscal Suture System - PMDA ID 371113_30300BZX00192000_A_01_02

NOVOSTITCH半月板縫合システム

Access comprehensive regulatory information for NOVOSTITCH Meniscal Suture System (NOVOSTITCH半月板縫合システム) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 371113_30300BZX00192000_A_01_02 and manufactured by Smith & Nephew Co., Ltd.. The device information was last updated on April 26, 2022.

This page provides complete registration details including device class (B0200), classification (plastic suture / プラスチック製縫合糸), 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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PMDA Official Data
Bilingual (EN/JP)
MD
B0200
371113_30300BZX00192000_A_01_02
MD
B0200
NOVOSTITCH Meniscal Suture System
NOVOSTITCH半月板縫合システム
PMDA ID: 371113_30300BZX00192000_A_01_02
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Intended Use / 使用目的
English

*This product is used to repair the function of a damaged meniscus in orthopedic or arthroscopic surgery. It is a plastic suture used for suturing and ligating soft tissues including sutures.

日本語 (Japanese)

*本 品は、整形外科的な手術又は関節鏡手術において損傷した半月板の機能を修復するために使用する。縫合器を含む軟組織の縫合・結紮に用いるプラスチック製の縫合糸である。

Device Classification / 分類
Device Type
MD
Device Class
B0200
Class Name (English)
plastic suture
Class Name (日本語)
プラスチック製縫合糸
Registration Information / 登録情報
PMDA ID
371113_30300BZX00192000_A_01_02
Last Update Date
April 26, 2022
Official Documents
Manufacturer / 製造販売業者
日本語 (Japanese)
製造販売/スミス・アンド・ネフュー株式会社
Product Names / 製品名
Market Name (English)
NOVOSTITCH Meniscal Suture System
Market Name (日本語)
NOVOSTITCH半月板縫合システム