21 HPV GenoArray Diagnostic Kit - FDA Registration 3794d2953621e481b2e3651486cd373e
Access comprehensive regulatory information for 21 HPV GenoArray Diagnostic Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3794d2953621e481b2e3651486cd373e and manufactured by Chaozhou Hybribio Biochemistry Ltd.. The device was registered on September 26, 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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3794d2953621e481b2e3651486cd373e
21 HPV GenoArray Diagnostic Kit
FDA ID: 3794d2953621e481b2e3651486cd373e
Device Classification
Brand Name
Hybribio
Registration Information
Analysis ID
3794d2953621e481b2e3651486cd373e
Registration Date
September 26, 2022
Manufacturer
Authorized Representative

