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Video Esophagoscope - FDA Registration 0d80ab8ecc3eaab0fb1559c1712d94fc

Access comprehensive regulatory information for Video Esophagoscope in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0d80ab8ecc3eaab0fb1559c1712d94fc and manufactured by Hoya Corporation PENTAX Miyagi Factory. The device was registered on July 26, 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
0d80ab8ecc3eaab0fb1559c1712d94fc
Video Esophagoscope
FDA ID: 0d80ab8ecc3eaab0fb1559c1712d94fc
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Device Classification
Brand Name
Pentax Medical
Registration Information
Analysis ID
0d80ab8ecc3eaab0fb1559c1712d94fc
Registration Date
July 26, 2022
Authorized Representative