HBsAg Rapid Test Cassette (Whole Blood/Serum/Plasma) - FDA Registration ef4fcaa14af399f2049f246c24b8a893
Access comprehensive regulatory information for HBsAg Rapid Test Cassette (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 ef4fcaa14af399f2049f246c24b8a893 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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ef4fcaa14af399f2049f246c24b8a893
HBsAg Rapid Test Cassette (Whole Blood/Serum/Plasma)
FDA ID: ef4fcaa14af399f2049f246c24b8a893
Device Classification
Brand Name
TVI
Registration Information
Analysis ID
ef4fcaa14af399f2049f246c24b8a893
Registration Date
October 19, 2022
Manufacturer
Authorized Representative

