Invivo nasal cannula - PMDA ID 670277_226ADBZX00172000_A_01_04

Access comprehensive regulatory information for Invivo nasal cannula (Invivo　鼻カニューレ) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 670277_226ADBZX00172000_A_01_04 and manufactured by Philips Japan Co., Ltd.. The device information was last updated on September 28, 2022.

This page provides complete registration details including device class (A5100), classification (Oxygen-supplying carbon dioxide-collecting nasal catheter / 酸素供給二酸化炭素収集経鼻カテーテル), 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.