EVIS EXERA lll COLONOVIDEOSCOPE - FDA Registration 96e7449100658beb43fc20ef67220ff9
Access comprehensive regulatory information for EVIS EXERA lll COLONOVIDEOSCOPE in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 96e7449100658beb43fc20ef67220ff9 and manufactured by Aizu Olympus Co., Ltd. The device was registered on November 11, 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.
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FDA Official Data
96e7449100658beb43fc20ef67220ff9
EVIS EXERA lll COLONOVIDEOSCOPE
FDA ID: 96e7449100658beb43fc20ef67220ff9
Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
96e7449100658beb43fc20ef67220ff9
Registration Date
November 11, 2021
Manufacturer
Authorized Representative

