Evis Exera III Duodenovideoscope & Accessories - FDA Registration 1cdb6eebd9ae5cc1b12bc35e5de4e8a5

Access comprehensive regulatory information for Evis Exera III Duodenovideoscope & Accessories in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1cdb6eebd9ae5cc1b12bc35e5de4e8a5 and manufactured by Aizu Olympus Co., Ltd. The device was registered on November 15, 2021.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.