HBsAg Rapid Test - FDA Registration 85062318038308566121d4d0ad9a3901
Access comprehensive regulatory information for HBsAg Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 85062318038308566121d4d0ad9a3901 and manufactured by CTK Biotech, Inc.. The device was registered on September 10, 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
85062318038308566121d4d0ad9a3901
HBsAg Rapid Test
FDA ID: 85062318038308566121d4d0ad9a3901
Device Classification
Brand Name
Aria Brand
Registration Information
Analysis ID
85062318038308566121d4d0ad9a3901
Registration Date
September 10, 2022
Manufacturer
Authorized Representative

