強膜プラグ鑷子 - PMDA ID 100707_27B1X00001900NKT_A_01_01
Access comprehensive regulatory information for 強膜プラグ鑷子 (強膜プラグ鑷子) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 100707_27B1X00001900NKT_A_01_01 and manufactured by Manufacturing and sales: R E Medical Corporation. The device information was last updated on February 13, 2025.
This page provides complete registration details including device class (A3600), classification (Ophthalmic tweezers / 眼科用ピンセット), 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.

