H.pylori Ab Combo Rapid Test - FDA Registration 5f49034d771eab95eab2579455e4f48f
Access comprehensive regulatory information for H.pylori Ab Combo Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5f49034d771eab95eab2579455e4f48f and manufactured by CTK Biotech, Inc.. The device was registered on September 01, 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
5f49034d771eab95eab2579455e4f48f
H.pylori Ab Combo Rapid Test
FDA ID: 5f49034d771eab95eab2579455e4f48f
Device Classification
Brand Name
Onsite
Registration Information
Analysis ID
5f49034d771eab95eab2579455e4f48f
Registration Date
September 01, 2022
Manufacturer
Authorized Representative

