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Sinus Kit - FDA Registration 7cfc625905f59de07548a20e688e767e

Access comprehensive regulatory information for Sinus Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7cfc625905f59de07548a20e688e767e and manufactured by Dentium Co., Ltd. The device was registered on November 12, 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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7cfc625905f59de07548a20e688e767e
Sinus Kit
FDA ID: 7cfc625905f59de07548a20e688e767e
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Device Classification
Brand Name
Dentium
Registration Information
Analysis ID
7cfc625905f59de07548a20e688e767e
Registration Date
November 12, 2022
Manufacturer
Authorized Representative