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Bioline HIV/Syphilis Duo - FDA Registration 6b25120811811faf0aeec94ca525f096

Access comprehensive regulatory information for Bioline HIV/Syphilis Duo in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6b25120811811faf0aeec94ca525f096 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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6b25120811811faf0aeec94ca525f096
Bioline HIV/Syphilis Duo
FDA ID: 6b25120811811faf0aeec94ca525f096
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Device Classification
Brand Name
Bioline
Registration Information
Analysis ID
6b25120811811faf0aeec94ca525f096
Registration Date
March 25, 2022
Authorized Representative