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HCV Ab Plus Rapid Test - FDA Registration 17381134d2e03974e9fb22660b1fc8bd

Access comprehensive regulatory information for HCV Ab Plus Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 17381134d2e03974e9fb22660b1fc8bd and manufactured by CTK Biotech. Inc.. The device was registered on November 18, 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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17381134d2e03974e9fb22660b1fc8bd
HCV Ab Plus Rapid Test
FDA ID: 17381134d2e03974e9fb22660b1fc8bd
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Device Classification
Brand Name
Onsite
Registration Information
Analysis ID
17381134d2e03974e9fb22660b1fc8bd
Registration Date
November 18, 2022
Manufacturer
Authorized Representative