Evis Lucera Elite Gastrointestinal Videoscope - FDA Registration a41a619a040c8f9f5df8481d6f8e6df4

Access comprehensive regulatory information for Evis Lucera Elite Gastrointestinal Videoscope in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a41a619a040c8f9f5df8481d6f8e6df4 and manufactured by Aizu Olympus Co., Ltd. The device was registered on March 18, 2022.

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.