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Malaria P.f/P.v Antigen Test - FDA Registration fa5982b65aecd3ac2e51c76160a8070f

Access comprehensive regulatory information for Malaria P.f/P.v Antigen Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fa5982b65aecd3ac2e51c76160a8070f and manufactured by Humasis Co.,Ltd. The device was registered on October 26, 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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fa5982b65aecd3ac2e51c76160a8070f
Malaria P.f/P.v Antigen Test
FDA ID: fa5982b65aecd3ac2e51c76160a8070f
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Device Classification
Brand Name
Humasis
Registration Information
Analysis ID
fa5982b65aecd3ac2e51c76160a8070f
Registration Date
October 26, 2022
Manufacturer
Authorized Representative