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hCG Combo Rapid Test - FDA Registration d609659efc4d32ce5f2212fd43459816

Access comprehensive regulatory information for hCG Combo Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d609659efc4d32ce5f2212fd43459816 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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d609659efc4d32ce5f2212fd43459816
hCG Combo Rapid Test
FDA ID: d609659efc4d32ce5f2212fd43459816
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Device Classification
Brand Name
Onsite
Registration Information
Analysis ID
d609659efc4d32ce5f2212fd43459816
Registration Date
September 01, 2022
Manufacturer
Authorized Representative