Blend-E XL THA Liner II - PMDA ID 510462_30200BZX00231000_A_02_01
Access comprehensive regulatory information for Blend-E XL THA Liner II (ブレンド−E XL THAライナII) in the Japan medical device market through Pure Global AI's free bilingual database. This MD medical device is registered under PMDA ID 510462_30200BZX00231000_A_02_01 and manufactured by Teijin Nakashima Medical Corporation. The device information was last updated on January 31, 2025.
This page provides complete registration details including device class (B0400), classification (Hip acetabular component / 人工股関節寛骨臼コンポーネント), 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.

