TaperGuard Reinforce Tracheal Tube
Japan·MD·A5100·Updated October 05, 2022- English
- This product is inserted into the trachea through the oral cavity or nasal cavity to secure the airway, administer inhalation anesthetics and medical gases, ventilate, etc. The combination of the tracheal tube and the stylet is for convenience. The purpose, efficacy or effect of "Stylet" is as described in the manufacturing and sales notification of the item.
- 日本語 (Japanese)
- 本品は、気道の確保又は吸入麻酔薬・医療用ガスの投与、換気等のため、口腔又は鼻腔から気管内に挿入する。なお、気管チューブとスタイレットの組合せについては、利便性のためのものである。「スタイレット」の使用目的、効能又は効果については、当該品目の製造販売届書に記載のとおり。
- Device Type
- MD
- Device Class
- A5100
- Class Name (English)
- Reinforced tracheal tube for ventilation
- Class Name (日本語)
- 換気用補強型気管チューブ
- PMDA ID
- 610015_225AABZX00038000_B_01_03
- Last Update Date
- October 05, 2022
- Official Documents
- View PDF (PMDA)
- English
- Covidien Japan Co., Ltd.
- 日本語 (Japanese)
- 製造販売／コヴィディエンジャパン株式会社
Access comprehensive regulatory information for TaperGuard Reinforce Tracheal Tube (TaperGuard リンフォース気管チューブ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 610015_225AABZX00038000_B_01_03 and manufactured by Covidien Japan Co., Ltd.. The device information was last updated on October 05, 2022.
This page provides complete registration details including device class (A5100), classification (Reinforced tracheal tube for ventilation / 換気用補強型気管チューブ), 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.