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Endoeye Flex Deflectable Videoscope - FDA Registration ac8b8470740a3b0c24186cacbb267b7f

Access comprehensive regulatory information for Endoeye Flex Deflectable Videoscope in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ac8b8470740a3b0c24186cacbb267b7f and manufactured by Aizu Olympus Co., Ltd. The device was registered on May 25, 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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ac8b8470740a3b0c24186cacbb267b7f
Endoeye Flex Deflectable Videoscope
FDA ID: ac8b8470740a3b0c24186cacbb267b7f
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Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
ac8b8470740a3b0c24186cacbb267b7f
Registration Date
May 25, 2022
Manufacturer
Authorized Representative