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Bioline HCV Rapid Assay - FDA Registration 55f8d7db179ee471d7e1bda96ecf3bbf

Access comprehensive regulatory information for Bioline HCV Rapid Assay in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 55f8d7db179ee471d7e1bda96ecf3bbf 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
55f8d7db179ee471d7e1bda96ecf3bbf
Bioline HCV Rapid Assay
FDA ID: 55f8d7db179ee471d7e1bda96ecf3bbf
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Device Classification
Brand Name
Bioline
Registration Information
Analysis ID
55f8d7db179ee471d7e1bda96ecf3bbf
Registration Date
March 25, 2022
Authorized Representative