Evis Lucera Elite Colonovideoscope - FDA Registration 5a26ee0b1861af9a59e8ce1ad2ec4695
Access comprehensive regulatory information for Evis Lucera Elite Colonovideoscope in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5a26ee0b1861af9a59e8ce1ad2ec4695 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.
Free Database
Powered by Pure Global AI
FDA Official Data
5a26ee0b1861af9a59e8ce1ad2ec4695
Evis Lucera Elite Colonovideoscope
FDA ID: 5a26ee0b1861af9a59e8ce1ad2ec4695
Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
5a26ee0b1861af9a59e8ce1ad2ec4695
Registration Date
March 18, 2022
Manufacturer
Authorized Representative

