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Endoscopic Ultrasound System - FDA Registration 6a8fdde18f89e1596cef841e6fde8d27

Access comprehensive regulatory information for Endoscopic Ultrasound System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6a8fdde18f89e1596cef841e6fde8d27 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on September 15, 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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6a8fdde18f89e1596cef841e6fde8d27
Endoscopic Ultrasound System
FDA ID: 6a8fdde18f89e1596cef841e6fde8d27
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Device Classification
Brand Name
FUJIFILM
Registration Information
Analysis ID
6a8fdde18f89e1596cef841e6fde8d27
Registration Date
September 15, 2022