Rapid Anti-HCV Test (Colloidal Gold) (Whole Blood/Serum/Plasma) - FDA Registration 7276c3c9844a7deebec0da3cbecbfefa
Access comprehensive regulatory information for Rapid Anti-HCV Test (Colloidal Gold) (Whole Blood/Serum/Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7276c3c9844a7deebec0da3cbecbfefa and manufactured by InTec PRODUCTS, INC.. The device was registered on October 30, 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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7276c3c9844a7deebec0da3cbecbfefa
Rapid Anti-HCV Test (Colloidal Gold) (Whole Blood/Serum/Plasma)
FDA ID: 7276c3c9844a7deebec0da3cbecbfefa
Device Classification
Brand Name
ADVANCED QUALITY
Registration Information
Analysis ID
7276c3c9844a7deebec0da3cbecbfefa
Registration Date
October 30, 2022
Manufacturer
Authorized Representative

