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Dengue NS1 Antigen Test - FDA Registration a12c73373aed158639944d4fbc59a555

Access comprehensive regulatory information for Dengue NS1 Antigen Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a12c73373aed158639944d4fbc59a555 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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FDA Official Data
a12c73373aed158639944d4fbc59a555
Dengue NS1 Antigen Test
FDA ID: a12c73373aed158639944d4fbc59a555
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DJ Fang

DJ Fang

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Device Classification
Brand Name
Humasis
Registration Information
Analysis ID
a12c73373aed158639944d4fbc59a555
Registration Date
October 26, 2022
Manufacturer
Authorized Representative