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HBsAg Combo Rapid Test - FDA Registration fe4555628a51fc5da35efb5d95e70a4a

Access comprehensive regulatory information for HBsAg Combo Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fe4555628a51fc5da35efb5d95e70a4a and manufactured by CTK Biotech, Inc.. The device was registered on October 19, 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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fe4555628a51fc5da35efb5d95e70a4a
HBsAg Combo Rapid Test
FDA ID: fe4555628a51fc5da35efb5d95e70a4a
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DJ Fang

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Device Classification
Brand Name
Aria Brand
Registration Information
Analysis ID
fe4555628a51fc5da35efb5d95e70a4a
Registration Date
October 19, 2022
Manufacturer
Authorized Representative