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Evis X1 Video System Center - FDA Registration 238c5e5cd939f1eafe27fe7ace50ecf2

Access comprehensive regulatory information for Evis X1 Video System Center in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 238c5e5cd939f1eafe27fe7ace50ecf2 and manufactured by Shirakawa Olympus Co.,Ltd. The device was registered on June 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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238c5e5cd939f1eafe27fe7ace50ecf2
Evis X1 Video System Center
FDA ID: 238c5e5cd939f1eafe27fe7ace50ecf2
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Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
238c5e5cd939f1eafe27fe7ace50ecf2
Registration Date
June 23, 2022
Authorized Representative