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Diagnostic X-ray System - FDA Registration 7806ce9c91f3caaefd01a1f71a8e81c7

Access comprehensive regulatory information for Diagnostic X-ray System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7806ce9c91f3caaefd01a1f71a8e81c7 and manufactured by DRGEM CORPORATION. The device was registered on December 30, 2021.

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
7806ce9c91f3caaefd01a1f71a8e81c7
Diagnostic X-ray System
FDA ID: 7806ce9c91f3caaefd01a1f71a8e81c7
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Device Classification
Brand Name
Fujifilm
Registration Information
Analysis ID
7806ce9c91f3caaefd01a1f71a8e81c7
Registration Date
December 30, 2021
Manufacturer
Authorized Representative