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AFIAS AMH - FDA Registration 8a412ec8d8d2ba5d4ec7cfa5366921ac

Access comprehensive regulatory information for AFIAS AMH in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8a412ec8d8d2ba5d4ec7cfa5366921ac and manufactured by Boditech Med Inc. The device was registered on June 30, 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
8a412ec8d8d2ba5d4ec7cfa5366921ac
AFIAS AMH
FDA ID: 8a412ec8d8d2ba5d4ec7cfa5366921ac
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Device Classification
Brand Name
AFIAS
Registration Information
Analysis ID
8a412ec8d8d2ba5d4ec7cfa5366921ac
Registration Date
June 30, 2022