boozy - PMDA ID 790130_13B3X10305THZ005_A_01_01
Access comprehensive regulatory information for boozy (ブージー) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 790130_13B3X10305THZ005_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 (A5200), classification (medical dilator / 医療用拡張器), 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.
Refers to a device used for expansion. Except for electric ones. This product is reusable.
拡張するために用いる器具をいう。電動式のものを除く。本品は再使用可能である。