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Bioline Dengue NS1 Ag - FDA Registration 2535d82e2100f4ed6a1ed1e2e8f5fbde

Access comprehensive regulatory information for Bioline Dengue NS1 Ag in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2535d82e2100f4ed6a1ed1e2e8f5fbde and manufactured by Abbott Diagnostics Korea Inc.. The device was registered on March 25, 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
2535d82e2100f4ed6a1ed1e2e8f5fbde
Bioline Dengue NS1 Ag
FDA ID: 2535d82e2100f4ed6a1ed1e2e8f5fbde
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DJ Fang

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Device Classification
Brand Name
Bioline
Registration Information
Analysis ID
2535d82e2100f4ed6a1ed1e2e8f5fbde
Registration Date
March 25, 2022
Authorized Representative