Nickel Titanium Archwire Super Elastic - PMDA ID 790122_21400BZY00169000_A_02_01

Access comprehensive regulatory information for Nickel Titanium Archwire Super Elastic (ニッケルチタンアーチワイヤー　スーパーエラスチック) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 790122_21400BZY00169000_A_02_01 and manufactured by Morimura Corporation. The device information was last updated on May 07, 2024.

This page provides complete registration details including device class (A5800), classification (Orthodontic wire / 歯列矯正用ワイヤ), 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.