Evis Exera III Video System Center & Xenon Light Source - FDA Registration 6c3a9e84b8e704e6454065fdfd890297
Access comprehensive regulatory information for Evis Exera III Video System Center & Xenon Light Source in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6c3a9e84b8e704e6454065fdfd890297 and manufactured by Shirakawa Olympus Co.,Ltd. The device was registered on March 23, 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.
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FDA Official Data
6c3a9e84b8e704e6454065fdfd890297
Evis Exera III Video System Center & Xenon Light Source
FDA ID: 6c3a9e84b8e704e6454065fdfd890297
Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
6c3a9e84b8e704e6454065fdfd890297
Registration Date
March 23, 2022
Manufacturer
Authorized Representative

