HBsAg Rapid Test Dipstick (Whole Blood/Serum/Plasma) - FDA Registration fa8f75d8c8cb05553e17795e63463e95
Access comprehensive regulatory information for HBsAg Rapid Test Dipstick (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 fa8f75d8c8cb05553e17795e63463e95 and manufactured by ACRO BIOTECH INC.. The device was registered on October 19, 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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fa8f75d8c8cb05553e17795e63463e95
HBsAg Rapid Test Dipstick (Whole Blood/Serum/Plasma)
FDA ID: fa8f75d8c8cb05553e17795e63463e95
Device Classification
Brand Name
TVI
Registration Information
Analysis ID
fa8f75d8c8cb05553e17795e63463e95
Registration Date
October 19, 2022
Manufacturer
Authorized Representative

